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The relief of post episiotomy pain

Comparison of the effects of lidocaine pomade , indomethacin suppository and mefenamic acid on the relief of post episiotomy pain in primiparous women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201104253078N7
Enrollment
90
Registered
2011-07-15
Start date
2011-05-31
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Post Episiotomy Pain. Pregnancy, childbirth and the puerperium

Interventions

Intervention 1: Group 1: The recipient of lidocaein pomad 2% on the episiotomy line and repeat every 6-8 hours until 24 hours after the delivery. Intervention 2: group 2: The recipient of 100 mg indom
Treatment - Drugs
Group 1: The recipient of lidocaein pomad 2% on the episiotomy line and repeat every 6-8 hours until 24 hours after the delivery
group 2: The recipient of 100 mg indomethacin suppository and repeat every 6-8 hours until 24 hours after the delivery
Group 3: The recipient of 250 mg mefenamic Acid capsule and repeat every 6-8 hours until 24 hours after the delivery

Sponsors

Research Council Of Shahrekord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion Criteria : The primiparous women with episiotomy Exclusion Criteria : The primiparous women with episiotomy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reduction of post episiotomy pain. Timepoint: 2-6012 and 24 hours after delivery. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Patient satisfaction. Timepoint: At the end of intervention. Method of measurement: Question of women.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoumeh Delaram

Shahrekord University Of medical Sciences

Mdelaram@skums.ac.irmasoumehdelaram@yahoo.com+98 38 1333 5648

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026