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COMPLETED
NCT07649668
PHASE4

Threatened Preterm Labour: Vaginal Progesterone Versus Nifedipine

Sponsor: Dr Mudassar Saeed Pansota

View on ClinicalTrials.gov

Summary

So, a number of studies have been conducted worldwide to find a suitable agent for arresting threatened preterm labor. The current study is planned to examine the effectiveness of nifedipine and progesterone in the treatment of threatened preterm labor (TPL). The result of this study will be used to recommend the best treatment modality in our population to reduce the risk of preterm labor

Official title: Efficacy of Vaginal Progesterone and Nifedipine in Inhibiting Threatened Preterm Labour

Key Details

Gender

FEMALE

Age Range

18 Years - 35 Years

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2025-11-30

Completion Date

2026-05-29

Last Updated

2026-06-16

Healthy Volunteers

No

Conditions

Interventions

DRUG

Vaginal progesterone 200mg daily

In Group B, participants will be instructed to use vaginal micronized progesterone tablets at a dosage of 200mg once daily or until reaching 37 weeks of gestational age or until cervical dilation exceeded 4cm (for a duration of 48 hours)

DRUG

Nifedipine 20 Mg

In Group A, participants will receive oral nifedipine at a dose of 20mg every 30 minutes for three doses initially, followed by long-acting nifedipine SR 20mg every 12 hours until reaching 37 weeks of gestational age or until cervical dilation exceeded 4cm (for a duration of 48 hours).

Locations (1)

Hilal-e-ahmar Hospital

Faisalabad, Punjab Province, Pakistan