NCT07075848

Brief Summary

Primigravida women are a high-priority population due to their increased risk of obstetric interventions and adverse outcomes compared to multiparous women. Research indicates that first-time mothers account for a disproportionate number of emergency cesarean sections and instrumental deliveries, often due to factors such as inadequate labor support or failure to progress

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
20mo left

Started Sep 2025

Typical duration for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress29%
Sep 2025Jan 2028

First Submitted

Initial submission to the registry

July 11, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 20, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

September 1, 2025

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2027

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2028

Last Updated

July 24, 2025

Status Verified

July 1, 2025

Enrollment Period

2.2 years

First QC Date

July 11, 2025

Last Update Submit

July 20, 2025

Conditions

Vaginal Delivery

Outcome Measures

Primary Outcomes (1)

  • The rate of vaginal delivery in cases

    24 hours

Study Arms (1)

study group

Procedure: vaginal delivery

Interventions

vaginal deliveryPROCEDURE

follow up of progress of labour

study group

Eligibility Criteria

Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Primigravida come in labour

You may qualify if:

  • Primigravida women admitted for delivery at the hospital
  • Singleton pregnancies.
  • Gestational age ≥ 28 weeks (to exclude preterm deliveries before viability).
  • Willingness to participate.

You may not qualify if:

  • Multiparous women.
  • Multiple pregnancies.
  • Women who decline to participate.
  • Deliveries occurring outside the specified study period.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

July 11, 2025

First Posted

July 20, 2025

Study Start

September 1, 2025

Primary Completion (Estimated)

November 1, 2027

Study Completion (Estimated)

January 1, 2028

Last Updated

July 24, 2025

Record last verified: 2025-07