NCT07685756Active, not recruiting
Cervical Ripening Balloon Compared With Vaginal Misoprostol for Cervical Ripening in Obese Woman at Term
Source: ClinicalTrials.gov · Last updated 6 Jul 2026
Brief summary (registry, in English)
Cervical ripening balloon compared with vaginal misoprostol for cervical ripening in obese woman at term
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 108 (estimated)
- First submitted
- 29 Jun 2026
- Start date
- 1 May 2026
- Primary completion date
- 31 Dec 2026
- Lead sponsor
- HUDDA Ahmad
- Diseases
- Obesity
- NCT number
- NCT07685756
What you commit to
- Study type: Interventional
- Planned participants: 108
- From 1 May 2026 to the primary completion date, 31 Dec 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- pregnancy with fetal demise congenital anomalies, History of uterine surgery In active labour \>4 cm dialated Obs complication History of uterine hyper stimulation and uterine rupture Feel malpresentation
Who the study is looking for
- obese women bmi \>30, Bishop score \<6 at time of ripening Singleton pregnancy Gestational age more than 37 weeks
Age in the registry: 18 years to 40 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Pakistan institute of medical sciences Islamabad Coordinator of this site? Confirm its status | Islamabad | Pakistan | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.