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A clinical study to assess Pain management using ultrasound guided nerve block for patients undergoing knee surgeries

Evaluation of Analgesic efficacy of Ultrasound guided Adductor canal block WITH 0.5% Ropivacine in patients undergoing knee surgeries - A randomised control trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/09/021182
Enrollment
70
Registered
2019-09-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M232- Derangement of meniscus due to oldtear or injury Health Condition 2: M239- Unspecified internal derangement of knee

Interventions

Intervention1: Adductor Canal Block: Ultrasound guided Adductor canal block for postoperative analgesia in patients undergoing knee surgeries Intervention2: Adductor Canal Block: Ultrasound guided Add

Sponsors

SRM medical college Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with ASA Physical Status I and II posted for knee surgeries under spinal anaesthesia 2. BMI ranging from 18-35 3. Age group of 18 â?? 60 year

Exclusion criteria

Exclusion criteria: 1.Patients who refuse the study 2. ASA 3 and 4 3. Drug allergy to ropivacine 4. Pregnancy 5. Bilateral knee surgeries 6. Revision surgeries

Design outcomes

Primary

MeasureTime frame
To evaluate the duration of anlagesia produced by Adductor canal blockTimepoint: 24 hrs after block—

Secondary

MeasureTime frame
To evaluate the average VAS score and analgesic consumption in the first 24 hours and side effects of blockTimepoint: 24 hours after block—

Countries

India

Contacts

Public ContactC R Saravanan

SRM medical college hospital and research centre

drcrsaravanan@gmail.com9884001153

Outcome results

None listed

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