The PAIN (Pelvic Area Injection for Numbness) Study

Last updated: May 30, 2025
Sponsor: Montefiore Medical Center
Overall Status: Active - Recruiting

Phase

4

Condition

Skin Wounds

Treatment

Bupivacaine with epinephrine arm

Bupivacaine

Bupivacaine and epinephrine

Clinical Study ID

NCT05972681
2023-14825
  • Ages > 18
  • Female
  • Accepts Healthy Volunteers

Study Summary

Postpartum pain can interfere with patient's ability to care for themselves, and their newborn, and untreated pain is associated with risk of greater opioid use, postpartum depression, and development of persistent pain. The research hypothesis of this study is that adding a locally injected analgesic, which will take effect once the epidural analgesia fades, may alleviate perineal pain and improve women's overall well-being and satisfaction.

The objective of this study is to determine if prolonged analgesia and higher rate of maternal satisfaction are found when bupivacaine with epinephrine infiltration is used for perineal repair as compared to sham injection in patients with pre-existing effective epidural analgesia at time of perineal laceration repair.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • >= 18 years old

  • Healthy with a singleton pregnancy

  • English or Spanish speaking

  • Ongoing functioning epidural throughout the laceration repair

  • Multiparous or nulliparous

  • Ability to consent for themselves

Exclusion

Exclusion Criteria:

  • Underwent an operative vaginal delivery and whose vaginal delivery was complicatedby a postpartum hemorrhage

  • Vaginal delivery was complicated by a postpartum hemorrhage

  • Have multiple gestations

  • Complaints of non-functional epidural

  • Allergic to bupivacaine and/or epinephrine

  • Epidural was a combined spinal-epidural (CSE)

  • Received an epidural top-off (bolus of local anesthetic injected into the epiduralcatheter) < 3 hours from the perineal repair

  • Experienced extreme pain at time of study consent (pain scale score > 3 on 0-10scale)

Study Design

Total Participants: 100
Treatment Group(s): 5
Primary Treatment: Bupivacaine with epinephrine arm
Phase: 4
Study Start date:
April 08, 2025
Estimated Completion Date:
July 31, 2026

Study Description

Perineal lacerations, the disruption of the skin, mucosa and sometimes muscles that happen commonly during vaginal birth secondary to stretching of the introitus; are present in more than 75% of all vaginal deliveries. These lacerations can be classified based on the location and depth (layers injured). However, the classification of these lacerations does not correlate necessarily with postpartum pain. Severe lacerations, as those compromising the external or internal anal sphincter are less common and associated with more postpartum pain.

It is common practice that only those lacerations causing bleeding, or distortion of normal pelvic anatomy are repaired. The repair of such lacerations at Montefiore Einstein is usually done using lidocaine for non-epiduralized patients; however, for patients with a functional epidural, no anesthetic agents are given locally to aid on long term pain control.

The prevalence of perineal lacerations is more than 75% of all vaginal deliveries. The repair of such lacerations in the institution is usually done using lidocaine for non-epiduralized patients versus no local injection in patients with a pre-existing epidural analgesia. The prevalence of epidural analgesia use among women who underwent vaginal delivery in cross-sectional study of over 2 million deliveries in the United States was 71.1%. Once the analgesic effect of the epidural analgesia fades, the laceration may cause uncontrolled postpartum pain which can affect both the physical and mental recovery period, extend hospital stays, and increase the potential for serious adverse reactions with pain medications.

Connect with a study center

  • Montefiore Medical Center

    Bronx, New York 10467
    United States

    Active - Recruiting

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