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Cervical Ripening Balloon Compared With Vaginal Misoprostol for Cervical Ripening in Obese Woman at Term

NCT07685756 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 108

Last updated 2026-07-06

No results posted yet for this study

Summary

Cervical ripening balloon compared with vaginal misoprostol for cervical ripening in obese woman at term

Conditions

  • Cervical Ripening

Interventions

DEVICE

Cervical folleys

We will compare effectiveness of cervical ripening with cervical folleys compared to misoprostol in obese women at term

DRUG

Misoprostol

We will compare effectiveness of ripening with misoprostol comoared with cervical folleys in obese women at term

Sponsors & Collaborators

  • HUDDA Ahmad

    lead OTHER_GOV

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-01
Primary Completion
2026-12-31
Completion
2027-06-01

Countries

  • Pakistan

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07685756 on ClinicalTrials.gov