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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03905980
Other study ID # 56
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 30, 2019
Est. completion date January 2020

Study information

Verified date July 2019
Source Cairo University
Contact Ahmed Maged, MD
Phone +201005227404
Email prof.ahmedmaged@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

women in their first pregnancy evaluated till delivery for associated risk factors for cesarean delivery


Description:

Evaluation of maternal , fetal, delivery place and health care provider rules to determine route of delivery in women during their first pregnancy


Recruitment information / eligibility

Status Recruiting
Enrollment 5000
Est. completion date January 2020
Est. primary completion date December 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- women in their first pregnancy

- Delivery between 37 and 42 weeks

- Singleton pregnancy _ cephalic presentation

Exclusion Criteria:

- women asked for CS on demand

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
vaginal delivery
pregnancy ended by vaginal delivery
Cesarean section
pregnancy ended by cesarean delivery

Locations

Country Name City State
Egypt Kasr Alainy medical school Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary route of delivery in primigravida at delivery
See also
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Active, not recruiting NCT03760718 - Chloroprocaine Lavage to Improve Outcomes Related to Operative Cesarean Delivery Early Phase 1
Active, not recruiting NCT04965779 - The Effect of Abdominal Binder Use on Postpartum Pain, Bleeding, and Breastfeeding Success in Cesarean Delivery Women N/A
Terminated NCT01687972 - INSORB Versus Subcuticular Sutures at Cesarean Section Phase 1
Withdrawn NCT01211431 - Post-cesarean Pain Control Via Continuous Infusion of Ropivacain et Diclogenac Into the Wound Versus Intathecal Morphine Phase 4
Completed NCT00991627 - Different Approaches to Maternal Hypotension During Cesarean Section Phase 4
Completed NCT00987701 - Perineuraxial Anesthesia Fluid Management and Infant Neurobehaviors N/A
Completed NCT01049477 - The Effects of Music Therapy on Women's Anxiety Before and During Cesarean Delivery N/A
Terminated NCT00524511 - Comparison Study of Wound Closure at Time of Cesarean Delivery: Dermabond Glue Versus Surgical Staples N/A
Terminated NCT00386477 - Vaginal Cleansing at Cesarean Delivery to Reduce Infection: A Randomized, Controlled Trial N/A
Completed NCT00375986 - A Comparison of Manual vs. Spontaneous Removal of the Placenta at Cesarean Section N/A
Completed NCT00517140 - Vaginal Birth After Caesarean Section - Effect on Maternal Psychosocial Function N/A
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