Trials / Not Yet Recruiting
Not Yet RecruitingNCT05785377
Neostigmine as an Adjuvant in Tranversus Abdominis Plane (TAP) Block in Cesarean Section Under Spinal Anesthesia
Efficacy of Neostigmine as an Adjuvant to Bupivacaine in Ultrasound-guided Transversus Abdominis Plane Block as a Postoperative Analgesia After Caesarean Delivery.
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 58 (estimated)
- Sponsor
- Mansoura University · Academic / Other
- Sex
- Female
- Age
- 19 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
Cesarean birth is a common surgical procedure. After cesarean birth, postsurgical pain may delay recovery, interfere with maternal-newborn bonding, and reduce the breastfeeding if not adequately controlled. Postpartum analgesia has become a common concern. Many adjuvant drugs used for peripheral nerve blocks as( N-methyl-d-aspartate (NMDA) receptor antagonists , Magnesium , Ephedrine , Dexamesathone , Fentanyl , Midazolam and Neostigmine) The potential of neostigmine as an adjuvant in peripheral nerve block is through its action to increase acetylcholine at muscarinic junctions of peripheral nerves. 500 mcg neostigmine was used as adjuvant to local anesthetic in an axillary brachial plexus block leads to decreased pain and less use of analgesics in the first 24 hours postoperatively with no incidence of adverse effects.
Detailed description
This prospective double-blinded randomized controlled study will be done on parturients that are scheduled for elective cesarean delivery under spinal anesthesia to assess the efficacy of neostigmine as an adjuvant to isobaric bupivacaine inTranversus abdominis plane (TAPB) for postoperative analgesia in cesarean section under spinal anesthesia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Bupivacaine-Neostigmine | 20 mL bupivacaine 0.25% plus 1 mL Neostigmine (500 mcg) |
| DRUG | Bupivacaine | 20 mL bupivacaine 0.25% plus 1 mL normal saline 0.9% |
Timeline
- Start date
- 2027-12-01
- Primary completion
- 2029-07-30
- Completion
- 2029-12-01
- First posted
- 2023-03-27
- Last updated
- 2026-02-17
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT05785377. Inclusion in this directory is not an endorsement.