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A study conducted to estimate the level of pain in normal vaginal delivery in first time pregnant females

An Observational Study To Estimate the Burden of Labour Pain in Primigravidas post normal vaginal delivery. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/03/107138
Enrollment
100
Registered
2026-03-30
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Indhira Gandhi medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Primigravidas Singleton pregnancy Age group of 18-35years Chephalic presentation with no cpd Pog of 37weeks or more Women in active stage of labor with cervical dilation more than 3cms

Exclusion criteria

Exclusion criteria: Multiple gestation Preterm pregnancy Malpresentation APH Medical complications like pre-clampsia or any neurological disease Foetal distress Women who received regional analgesia( e.g., Epidural) Women who have undergone Emergency or Elective LSCS Patients who refused to participate

Design outcomes

Primary

MeasureTime frame
To estimate the pain levels in primigravidas post normal vaginal deliveryTimepoint: 24hours post normal vaginal delivery—

Secondary

MeasureTime frame
To relate patient satisfaction score with duration of pain scoresTimepoint: After 24 hours post normal vaginal delivery—

Countries

India

Contacts

Public ContactNAVVOTHU SAI NIKHIL

Indhira Gandhi Medical College

Kartik.syal@gmail.com9418485155

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026