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lidocaine spray, pomade and infiltrative form in episiotomy repair

The comparison of efficiency of lidocaine spray, pomade and infiltrative form in episiotomy repair

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
PACTR
Registry ID
PACTR201811710982025
Enrollment
300
Registered
2018-11-30
Start date
2018-11-29
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

The pain of the episiotomy

Interventions

Experimental pomade group
Experimental spray group
Control infiltrative group

Sponsors

MOGADISHU SOMALI TURKEY RECEP TAYYIP ERDOGAN EDUCATION AND RESEARCH HOSPITAL
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Pregnant women aged 18-40. 2. Women who have 37-42 weeks of pregnancy. 3. Women with nulliparous pregnancy. 4. Pregnant women with BMI <35. 5. Pregnant women who agree to participate in the study. 6. Pregnant women with postpartum obstetric episiotomy.

Exclusion criteria

Exclusion criteria: 1. Multiparity. 2. Women with BMI> 35. 3. Women who have had vaginal surgery before. 4. Women who do not want to participate in the study. 5. Preterm births.

Design outcomes

Primary

MeasureTime frame
Pain levels will be recorded by applying VAS (visual analog scoring system) at 0. 4. 8. 12. 24. hours of episiotomy repair.

Secondary

MeasureTime frame
Latent and active phase duration first stage of labor, duration of second stage of labor and duration of 3rd stage, episiotomy repair time, additional analgesic requirement during procedure and after, duration of discharge, maternal and fetal complications will be recorded.

Countries

Somalia

Contacts

Public ContactSamaara Hassan

Miss.

samaara010@gmail.com+252615937497

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026