Combined Method for Induction of Labor

Status

UNKNOWN

Phases

Phase 2

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02685085

Enrollment

300

Registered

2016-02-18

Start date

2016-02-29

Completion date

2016-08-31

Last updated

2016-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Induced Labor

Brief summary

Induction of labor is performed via the vaginal misorostol 25 ug/ 6 hours and intracervical foley's cather administration and both techniques performed together.

Interventions

DRUGMisoprostol ( Prostaglandin E2)

DEVICEFoley's catheter

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 45 Years

Healthy volunteers

Yes

Inclusion criteria

* females presenting for induction of labor

Exclusion criteria

* previous cesarean section * previous uterine scars e.g. myomectomy * refusal to participate in the study

Design outcomes

Primary

Measure	Time frame
Duration of induction of labor	24 hours

Countries

Egypt

Contacts

Primary ContactDina MR Dakhly, MD

dinadakhly@gmail.com01003498919

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026