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[PDF] Top 20 Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial

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Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial

Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial

... a dressing after the first 24 postoperative hours could be convenient for patients, allowing them to carry out their personal hygiene more easily ...of breast cancer treatment, we hypothesize that ... See full document

6

The impact of an online patient decision aid for women with breast cancer considering immediate breast reconstruction: study protocol of a multicenter randomized controlled trial

The impact of an online patient decision aid for women with breast cancer considering immediate breast reconstruction: study protocol of a multicenter randomized controlled trial

... for study participation by their treating surgical oncologist, nurse specialist or breast cancer nurse during a regular pre-surgical treatment consultation in which the possibility of breast ... See full document

12

Transversus abdominis plane block following abdominally based breast reconstruction: study protocol for a randomized controlled trial

Transversus abdominis plane block following abdominally based breast reconstruction: study protocol for a randomized controlled trial

... It is well-known that adequate analgesia decreases the incidence of cardiopulmonary complications and in-hospital deaths [6]. Several authors have investigated methods of improving postoperative analgesia with the use of ... See full document

8

The Multi Centre Canadian Acellular Dermal Matrix Trial (MCCAT): study protocol for a randomized controlled trial in implant based breast reconstruction

The Multi Centre Canadian Acellular Dermal Matrix Trial (MCCAT): study protocol for a randomized controlled trial in implant based breast reconstruction

... the BREAST-Q is a validated, reliable assessment of QOL that should provide a robust measure of satisfac- ...as breast cancer stage (prophylactic versus in situ versus invasive breast cancer), it ... See full document

12

CONCEPTT: Continuous Glucose Monitoring in Women with Type 1 Diabetes in Pregnancy Trial: A multi center, multi national, randomized controlled trial   Study protocol

CONCEPTT: Continuous Glucose Monitoring in Women with Type 1 Diabetes in Pregnancy Trial: A multi center, multi national, randomized controlled trial Study protocol

... two randomized trials in pregnancy are conflicting. In a UK trial of 71 women with type 1 and type 2 diabetes, ran- domized to wearing a masked CGM every 4–6 weeks compared to standard care with HGM, the ... See full document

8

Which dressing do donor site wounds need?: study protocol for a randomized controlled trial

Which dressing do donor site wounds need?: study protocol for a randomized controlled trial

... six-armed randomized clinical trial is being carried out in the ...mean time to complete wound ...silicone dressing, or paraffin ...this trial are ...the protocol as supplied by ... See full document

6

The effects of combined exercise intervention based on Internet and social media software for postoperative patients with breast cancer: study protocol for a randomized controlled trial

The effects of combined exercise intervention based on Internet and social media software for postoperative patients with breast cancer: study protocol for a randomized controlled trial

... This study is a RCT with an intervention time of 12 weeks. Trial participants were recruited starting in August 2017 and the data will be analyzed after the sample size is achieved according ... See full document

8

Impact of exercise training on cardiotoxicity and cardiac health outcomes in women with breast cancer anthracycline chemotherapy: a study protocol for a randomized controlled trial

Impact of exercise training on cardiotoxicity and cardiac health outcomes in women with breast cancer anthracycline chemotherapy: a study protocol for a randomized controlled trial

... the time-domain (standard deviation of successive normal R-R (SDNN), and root mean square of successive normal R-R (RMSSD)) and frequency-domain indices (low-frequency spectral component (LF), and high-frequency ... See full document

11

Study protocol: a single blind, multi center, randomized controlled trial comparing dynamic intraligamentary stabilization, internal brace ligament augmentation and reconstruction in individuals with an acute anterior cruciate ligament rupture: LIBRƎ stud

Study protocol: a single blind, multi center, randomized controlled trial comparing dynamic intraligamentary stabilization, internal brace ligament augmentation and reconstruction in individuals with an acute anterior cruciate ligament rupture: LIBRƎ study

... ery time and consequently a reduced need for costly physiotherapy, and faster return to work and sports [17, 20, ...one study has been published which compared DIS with the ACL reconstruction ...the ... See full document

13

Application time for postoperative wound dressing following breast augmentation with implants: study protocol for a randomized controlled trial

Application time for postoperative wound dressing following breast augmentation with implants: study protocol for a randomized controlled trial

... in breast augmentation is warranted, as this incision acts as a gateway for microor- ganisms present on the surrounding skin or in external sources of ...of breast implants are most commonly placed in the ... See full document

6

2017 WSES and SICG guidelines on acute calcolous cholecystitis in elderly population

2017 WSES and SICG guidelines on acute calcolous cholecystitis in elderly population

... hour after severe sepsis and septic shock are recognized, use of broad-spectrum agents with good penetration into the presumed site of infection, and reassessment of the antimicrobial regi- men daily to optimize ... See full document

16

Expanding care for perinatal women with depression (EXPONATE): study protocol for a randomized controlled trial of an intervention package for perinatal depression in primary care

Expanding care for perinatal women with depression (EXPONATE): study protocol for a randomized controlled trial of an intervention package for perinatal depression in primary care

... the trial will be in accordance with CONSORT guide- lines for cluster randomized trials [46, ...as randomized without imputation of miss- ing data, and with due emphasis placed on confidence ... See full document

9

Assessment of DHA on reducing early preterm birth: the ADORE randomized controlled trial protocol

Assessment of DHA on reducing early preterm birth: the ADORE randomized controlled trial protocol

... at study entry) http:// ...teams after the data are entered into the eResearch by reviewing source ...the trial and retained ac- cording to the appropriate ... See full document

16

The effects of parental components in a trauma focused cognitive behavioral based therapy for children exposed to interparental violence: study protocol for a randomized controlled trial

The effects of parental components in a trauma focused cognitive behavioral based therapy for children exposed to interparental violence: study protocol for a randomized controlled trial

... min. After each session, the thera- pists of both the parent and child groups will evaluate the session and share information about children’ s as well as parents’ ... See full document

18

Narrative exposure therapy for immigrant children traumatized by war: study protocol for a randomized controlled trial of effectiveness and mechanisms of change

Narrative exposure therapy for immigrant children traumatized by war: study protocol for a randomized controlled trial of effectiveness and mechanisms of change

... with time, for some, posttraumatic stress symptoms due to war experi- ences in childhood show persistence for years and even decades [6, 7], and have been shown to be related to a number of psychological and ... See full document

14

Evaluation of a nurse mentoring intervention to family caregivers in the management of delirium after cardiac surgery (MENTOR D): a study protocol for a randomized controlled pilot trial

Evaluation of a nurse mentoring intervention to family caregivers in the management of delirium after cardiac surgery (MENTOR D): a study protocol for a randomized controlled pilot trial

... pilot study protocol will enable us to build a larger study with a sufficient number of participants to ensure adequate statistical power that can potentially add to the knowledge on de- lirium ... See full document

13

Smart-Phone Obesity Prevention Trial for Adolescent Boys in Low-Income Communities: The ATLAS RCT

Smart-Phone Obesity Prevention Trial for Adolescent Boys in Low-Income Communities: The ATLAS RCT

... criteria aimed to identify boys at in- creased risk of obesity based on their physical activity and screen behaviors. This approach was selected to reduce the potential for weight stigmatization, which may occur if ... See full document

11

A combination of multimodal physical exercises in real and virtual environments for individuals after chronic stroke: study protocol for a randomized controlled trial

A combination of multimodal physical exercises in real and virtual environments for individuals after chronic stroke: study protocol for a randomized controlled trial

... [16] study, the control group performed 1 h of occupational therapy per session, and the experimental group performed 30 min of occupa- tional therapy plus 30 min of virtual ... See full document

11

A phase 1/2 trial to evaluate the pharmacokinetics, safety, and efficacy of NI 03 in patients with chronic pancreatitis: study protocol for a randomized controlled trial on the assessment of camostat treatment in chronic pancreatitis (TACTIC)

A phase 1/2 trial to evaluate the pharmacokinetics, safety, and efficacy of NI 03 in patients with chronic pancreatitis: study protocol for a randomized controlled trial on the assessment of camostat treatment in chronic pancreatitis (TACTIC)

... a randomized, placebo-con- trolled trial in 287 subjects experienced “marked improve- ment,” which was defined on a 6-point scale (markedly improved, improved, slightly improved, unchanged, wors- ened, and ... See full document

7

Mifepristone and misoprostol versus misoprostol alone for uterine evacuation after early pregnancy failure: study protocol for a randomized double blinded placebo controlled comparison (Triple M Trial)

Mifepristone and misoprostol versus misoprostol alone for uterine evacuation after early pregnancy failure: study protocol for a randomized double blinded placebo controlled comparison (Triple M Trial)

... retrospective study design [14]. A double- blinded pilot pilot study performed by our research group in- cluding women with EPF between 6 and 14 weeks of gesta- tion after a minimum of 1 week of ... See full document

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