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Comparison of postoperative pain relief using two methods of ropivacaine injections in patients undergoing abdominal surgeries: a prospective randomized study.

Effect of long-axis versus conventional rectus abdominis sheath block with ropivacaine on post-operative analgesia in patients undergoing midline laparotomies: a prospective randomized study. - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058393
Enrollment
64
Registered
2023-10-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere Health Condition 2: K566- Other and unspecified intestinal obstruction Health Condition 3: K420- Umbilical hernia with obstruction,without gangrene

Interventions

Intervention1: Long-axis rectus abdominis sheath block: Patients randomised to long-axis rectus abdominis sheath block will be given long-axis rectus abdominis sheath block bilaterally and bilateral T

Sponsors

All India Institute of Medical Science Bhubaneswar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I & II patients (age – 18 to 70 years) undergoing midline laparotomies Patients who can understand and provide a valid consent for the procedure and can understand and are willing to report the pain using NRS score.

Exclusion criteria

Exclusion criteria: Patients not willing to give consent Patients undergoing re-do surgeries Patients with known allergy to study drug Patients with psychiatric disorders Patients who have had pre-operative opioid consumption Patients on chronic pain medication Severe cardiac or pulmonary dysfunction

Design outcomes

Primary

MeasureTime frame
To compare the time to the first demand of rescue analgesia (NRS score more than or equal to 4) in long-axis versus conventional rectus abdominis sheath blockTimepoint: Within first 24 hours post extubation after surgery—

Secondary

MeasureTime frame
To compare intra-operative opioid requirement To compare the NRS score at 1 hour, 3 hours, 6 hours, 12 hours, 18 hours & 24 hours post extubation after the surgery To compare the mean NRS in 24 hours To compare the total dose of rescue tramadol required in the first 24 hrs To compare the patient satisfaction score To compare the complicationsTimepoint: Total intra-operative opioid requirement by the end of surgery. NRS score at 1 hour, 3 hours, 6 hours, 12 hours, 18 hours & 24 hours post extubation after the surgery. Other parameters by first 24 hours post extubation after surgery—

Countries

India

Contacts

Public ContactDr Anakha Fatima Kunjali

All India Institute of Medical Science Bhubaneswar

anaes_sritam@aiimsbhubaneswar.edu.in8951614718

Outcome results

None listed

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