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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03080506 |
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Date of registration:
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07/03/2017 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Abdominal Binder Following Cesarean Delivery
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Scientific title:
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Effect of Elastic Abdominal Binder on Pain and Functional Recovery After Cesarean Delivery: a Randomized Controlled Trial |
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Date of first enrolment:
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April 18, 2017 |
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Target sample size:
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180 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03080506 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Supportive Care. Masking: Single (Investigator).
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Phase:
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N/A
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Countries of recruitment
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Thailand
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Contacts
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Name:
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Kittipat Charoenkwan, MD, MSc |
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Address:
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Telephone:
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Email:
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Affiliation:
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Chiang Mai University |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Pregnant women undergoing cesarean delivery
Exclusion Criteria:
- Cesarean hysterectomy
- Intraoperative accidental injury to urinary or gastrointestinal organs
- Postoperative admission to intensive care unit (ICU)
- Postoperative intraperitoneal drain placement
- Unable to understand and follow oral/written instructions
- Severe neuromuscular or circulatory disorders
- Pulmonary diseases
Age minimum:
18 Years
Age maximum:
45 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Cesarean Section Complications
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Intervention(s)
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Device: Elastic abdominal binder
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Primary Outcome(s)
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Daily average postoperative pain scores
[Time Frame: An average of pain scores at 8:00 am and 4:00 pm, up to 7 days postoperation]
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Postoperative functional recovery
[Time Frame: In the morning of postoperative day 3]
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Secondary Outcome(s)
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Quality of life
[Time Frame: In the morning of postoperative day 3]
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Postoperative complications
[Time Frame: In the morning, up to 7 days postoperation]
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Secondary ID(s)
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OBG-2559-04139
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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