comparative evaluation of plain lidocaine and bupivacaine-lidocaine infiltration for episiotomy and episiorraphy pain relieve at Federal Medical Center Owo. A randomized control trial.

Comparative evaluation of plain lidocaine and bupivacaine-lidocaine infiltration for episiotomy and episiorraphy pain relieve at Federal Medical Center Owo. A randomized control trial.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202504557727723

Enrollment

140

Registered

2025-04-15

Start date

2024-06-29

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Anaesthesia

Interventions

plain lidocaine and bupivacaine lidocaine combination for episiotomy relieve

BUPIVACAINE LIDOCAINE

Lidocaine

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: All consenting patients within the ages of 18 to 35 years who require episiotomy.

Exclusion criteria

Exclusion criteria: 1. Patient’s refusal 2. History of cardiac disease or any co-morbid state 3. History of allergy to local anesthesia, especially amides 4. Body mass index at booking 30 kg/m2

Design outcomes

Primary

Measure	Time frame
1.Episiorraphy and post-episiorraphy analgesic effect with verbal rating scale assessment 2.Time for the first analgesic request 3.Dose of analgesic required in 24 hours	—

Secondary

Measure	Time frame
1. Patients with post-episiorrhaphy pain 2. Satisfaction of the patients	—

Countries

Nigeria

Contacts

Public ContactVERONICA SALAJA

PUBLIC RESEARCHER

ibukunsalaja23@gmail.com+2347062448255

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026