Skip to content

Comparing different strengths of a local anaesthetic drug to relieve pain after hip replacement surgery when given through a nerve block near the groin

Comparison of the efficacy of Suprainguinal fascia iliaca block performed with different concentrations of ropivacaine on postoperative analgesia after total hip replacement surgery: A randomized, double blinded clinical trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084760
Enrollment
120
Registered
2025-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: M248- Other specific joint derangements,not elsewhere classified

Interventions

Intervention1: Ropivacaine(0.1%): Adminstration of 0.1% concentration of ropivacaine via USG guided suprainguinal fascia iliaca block preoperatively before spinal anaesthesia and monitoring done for p

Sponsors

Dr Shipra Goyal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Standards Association (ASA) grade I-II; Patients undergoing elective surgeries of total hip replacement

Exclusion criteria

Exclusion criteria: 1)Patient refusal 2)Previous coagulation or bleeding disorder, 3)Receiving anticoagulant therapy, 4)Allergy/sensitivity to local anaesthetics (LAs) and/or opioids )Infection in the procedure area

Design outcomes

Primary

MeasureTime frame
To assess the mean duration of analgesia (time to first request for rescue analgesia)Timepoint: To assess the mean duration of analgesia time in post operative period till patient request for analgesia

Secondary

MeasureTime frame
1)To assess severity of postoperative analgesia as pain scores at rest & during movement (measured using the NRS) 2)Total mean dose of rescue analgesia 3)To assess motor block (by using Oxford scale) 4)To assess adverse effects, including nausea, vomiting & local anesthetic systemic toxicity 5)To assess patient satisfaction with Likert scale Timepoint: 1)assessed in postoperative period from baseline 2)assessed for 24 hours of postoperative period from baseline 3)assessed for 24 hours of postoperative period from baseline 4)assessed for 24 hours of postoperative period from baseline 5)assessed for 24 hours of postoperative period from baseline

Countries

India

Contacts

Public ContactDr Vandana Sharma

Dr S N medical college

sarita.janweja@gmail.com9829116420

Outcome results

None listed

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