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NCT00550888 Clinical Trial

Comparison of Uterine Exteriorization Versus in Situ Repair at Cesarean Section: a Randomized Clinical Trial

Cesarean Section Clinical Trial

— EXT  

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00550888
Other study ID # IMIP1234
Secondary ID
Status Completed
Phase Phase 3
First received October 29, 2007
Last updated June 8, 2010
Start date August 2005
Est. completion date August 2007

Study information
Verified date August 2007
Source Instituto Materno Infantil Prof. Fernando Figueira
Contact n/a
Is FDA regulated No
Health authority Brazil: Ministry of Health
Study type Interventional

Clinical Trial Summary

There is no difference between extra-abdominal or in situ suture of the uterus in cesarean section.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date August 2007
Est. primary completion date
Accepts healthy volunteers
Gender Female
Age group 13 Years to 44 Years
Eligibility Inclusion Criteria:

- indication of cesarean section

- gestational age > 24 weeks

Exclusion Criteria:

- two or more cesarean sections

- chorioamnionitis

- hemorrhagic complications

- unable to consent

- previous abdominal surgery

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject)

Related Conditions & MeSH terms

Intervention

Procedure:
• suture techniques

Locations
Country Name City State
Brazil IMIP Prof. Fernando Figueira Recife Pernambuco

Sponsors (1)
Lead Sponsor Collaborator
Instituto Materno Infantil Prof. Fernando Figueira

Country where clinical trial is conducted

Brazil, 

Outcome
Type Measure Description Time frame Safety issue
Primary endometritis within the first 30 days after surgery
Secondary nausea and vomiting during surgery, mean operative time, estimated intraoperative blood loss, number of surgical sutures for uterine repair, pain postoperative, number of postoperative analgesic doses, surgical site infection from surgery to 30 days after surgery
See also
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Terminated NCT05051150 - Epinephrine Infusion for Prophylaxis Against Maternal Hypotension During Caesarean Section Phase 4
Terminated NCT03695172 - Comparison of TAP, Anterior QL, or ESP Block for Elective Cesarean Section Phase 4
Recruiting NCT06247852 - Persistent Pain After Cesarean Delivery - A Danish Multicenter Cohort Study
Completed NCT06012747 - Pain After Cesarean Section - A Danish Multicenter Cohort Study.
Not yet recruiting NCT05187520 - Naldebain for Control of Post-Cesarean Section Pain Phase 2
Not yet recruiting NCT04999670 - Fascial Closure and Post-caesarean Pain N/A