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This is a clinical study for evaluation of pain relief following piles surgery using ultrasound guided pudendal nerve block.

A comparative evaluation of ultrasound guided pudendal nerve block for postoperative analgesia in patients undergoing stapled hemorrhoidectomy. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069307
Enrollment
70
Registered
2024-06-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Ultrasound guided pudendal nerve block.: Patients will receive 15 mls of injection ropivacaine 0.3% with 4 mg of dexamethasone on each side under ultrasound guidance using 22 G echogeni

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Patients undergoing stapled hemorrhoidectomy under GA • American society of anesthesiology (ASA) grade 1 and 2 patients.

Exclusion criteria

Exclusion criteria: 1. Patient refusal 2. ASA 3 and above 3. Patients with features of local infection at the site of block 4. Patients with history of bleeding disorder or on anticoagulant therapy 5. Patients with known allergy to local anesthetic drugs 6. Patients with mental illness 7. Patients with neuromuscular disorders

Design outcomes

Primary

MeasureTime frame
Time of requirement of first rescue opioid analgesic.Timepoint: 0 , 4 , 8 ,12 and 24 hours

Secondary

MeasureTime frame
1. To compare overall requirements for Opioids in 24 hours. 2. Pain score. 3. Patient satisfaction score. 4. Side effects like nausea, vomiting and sedation. Timepoint: during first 24 hours.

Countries

India

Contacts

Public ContactDr Divesh Arora

Asian Hospital Faridabad

akchaudhary798@gmail.com7037134666

Outcome results

None listed

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