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NCT Number: NCT06935669

Analgesic Effect of Bupivacaine Plus Ketamine Versus Bupivacaine Alone in Transversalis Fascia Plane Block

The objective of this study is to compare the efficacy of transversalis fascia plane block using bupivacaine and ketamine versus bupivacaine alone for pain management after cesarean section under spinal anaesthesia.

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Key information

Age range

21 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1

Primary location

Ain Shams University faculty of medicine

Cairo, Egypt

Location contact

Ain Shams University faculty of medicine Ain Shams Universit faculty of medicine

CONTACT

[email protected]

02 26837673

About this study

Cesarean section (CS) is one of the most common surgeries and usually causes moderate to severe pain for up to 48 h. The rate of CS, which is a life-saving surgical procedure in cases of certain complications that occur during pregnancy and birth, has exceeded 20% worldwide Pain control after CS has crucial importance, especially in the first 24 h, to facilitate early ambulation and the establishment of breastfeeding. Insufficient analgesia in the postoperative period may cause a number of undesirable effects, such as patient discomfort, thromboembolism due to extended immobilization, and increased pulmonary secretions resulting in complications The well-known side effects of analgesic morphine as nausea, vomiting, itching and sedation, may interfere with the interaction between mother and child, breastfeeding and post-partum experience in a dose-dependent manner. However, a number of alternative strategies have been described in order to reduce morphine consumption post-operatively .

The mode and type of analgesia should be safe and effective. A stimulus caused by a lesion in tissue or organs during surgery is the cause of postoperative pain .

The primary source of pain after abdominal surgeries, including CS, are the anterior abdominal wall and abdominal viscera, and blocking these areas could provide proper postoperative analgesia .

Recently, the application of fascial plane blocks has increased due to the widespread use of ultrasound among anesthesiologists and the avoidance of opioids in a multimodal analgesic strategy. Different regional anesthetic techniques have been introduced, including ilioinguinal nerve blocks, abdominal field blocks, Transversalis Fascia Plane (TFP) blocks, and Transversus Abdominis Plane (TAP) blocks to alleviate pain from the abdominal wall incision .

Transversalis Fascia Plane, performed in the posterior axillary line, blocks branches of L1 nerve roots, including ilioinguinal and iliohypogastric nerves. This method has been used to control postoperative pain in patients undergoing different lower abdominal surgeries A variety of anesthetic agents such as bupivacaine, levobupivacaine, and ropivacaine are commonly used in TAP blocks. These drugs provide short-term analgesia and primarily alleviate somatic pain. To extend the duration of analgesic efficacy, various adjuvants such as opioids, ketamine, clonidine, and alpha-2 agonists like dexmedetomidine have been added .

Bupivacaine is one of the widely used local analgesics. ketamine affects pain modulation through multiple mechanisms of action. It is a non-competitive N-methyl-d-aspartate (NMDA) receptor antagonist, which exerts an anti-hyperalgesic effect by decreasing central sensitization and reducing the wind-up phenomenon in the postoperative period .

The aim of this study is to investigate the effect of transversalis fascia plane block using bupivacaine plus ketamine on postoperative pain compared to bupivacaine alone in patients undergoing cesarean section under spinal anaesthesia.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aging ≥ 21 years to ≤ 45.
  • Patients undergoing cesarean section under spinal anesthesia.
  • American Society of Anesthesiologists (ASA) physical statusphysical status classes II.

Exclusion criteria

  • Patient's refusal of procedure or participation in the study.
  • Coagulopathy and bleeding disorders.
  • Use of chronic pain medications.
  • Pregnancy-induced hypertension or diabetes.
  • Evidence of Local skin infections at site of injection.
  • Body mass index >40kg/m2
  • A history of relevant local anesthetic allergy.

Treatment and study plan

ketamine

Drug

Patients in this group will receive a transversalis fascia plane block using a combination of bupivacaine and ketamine.

Other names: Ketalar

Bupivacaine

Drug

Control group to evaluate the additional effect of ketamine in the experimental arm.

Other names: Marcaine

Bupivacain

Drug

Patients in this group will receive a transversalis fascia plane block using a combination of bupivacaine and ketamine.

Other names: Marcaine

Primary outcomes

  1. The mean VAS pain on movement will be recorded as the primary outcome of the study

    Time frame: day 1

    Pain intensity will be assessed using the Visual Analog Scale (VAS), where 0 = no pain and 10 = worst pain.

    Patients will report their pain levels at rest and during movement at 24 hours after the transversalis fascia plane block.

    The mean VAS score will be compared between the ketamine + bupivacaine group and the bupivacaine-only group.

Secondary outcomes

  1. Time to first rescue analgesia will be recorded

    Time frame: Day 1

    Time (in minutes/hours) from the completion of the transversalis fascia plane block to the administration of the first dose of rescue analgesia will be recorded.

    Rescue analgesia will be given when the patient reports a VAS score ≥ 4 or requests additional pain relief.

    A longer time to first rescue analgesia in the ketamine + bupivacaine group would indicate prolonged analgesic duration compared to the bupivacaine-only group.

  2. total requirements of rescue analgesia Nalbuphine over the first 24 hours postoperative will be recorded

    Time frame: Day 1

    Rescue analgesia will be given when the patient reports a VAS score ≥ 4 or requests additional pain relief.

Study contacts

Contact information is provided by the study sponsor or research team.

Ahmed Ad MAHMOUD Ebrahim elgamal

CONTACT

[email protected]

+02 01159008254

Eman Sh Abdelmaqsoud

CONTACT

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Official study title

Randomised Controlled Clinical Trial Analgesic Effect of Bupivacaine Plus Ketamine Versus Bupivacaine Alone in Transversalis Fascia Plane Block After Cesarean Section Under Spinal Anaesthesia

Acronym: TFBP

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 20, 2025
Registry last updated
Apr 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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