Skip to content

Control of pain ,following a Total knee replacement surgery ,using different modalities

The additive effect of adductor canal block in post op analgesia for Total Knee - A randomized controlled trial. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021502
Enrollment
40
Registered
2019-10-01
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: M170- Bilateral primary osteoarthritis of knee Health Condition 2: M174- Other bilateral secondary osteoarthritis of knee Health Condition 3: M175- Other unilateral secondary osteoarthritis of knee Health Condition 4: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: Intervention is periarticular injection plus adductor canal block for patients undergoing Total knee Replacement surgery Comparator is periarticular injection alone in a Total knee Repl

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients undergoing Total Knee Replacement surgery

Exclusion criteria

Exclusion criteria: Elderly more than 80 years Revision/Complex Total Knee Replacement Patients with history of Arrhythmia/Cardiac complications Those not willing to give consent.

Design outcomes

Primary

MeasureTime frame
Pain - as estimated by the patients using a numeric pain score till 72 hours post-operativelyTimepoint: 1 At 24 hours after surgery 2 At 48 hours after surgery 3 At 72 hours after surgery

Secondary

MeasureTime frame
1 Quadriceps strength on post operative day 2,3,5,10 and 3 months- as measured with a standardized load cell,to be recorded by the physiotherapist 2 Time taken to do a Straight Leg Raise with 0 degree lag to a count of 10- without braces - while supine in bed - for each knee 3 Morphine consumption post operatively(Unilateral knees only) 4.Overall satisfaction with pain control peri-operatively ( at time of discharge) (scale of 0-10) Timepoint: 1 At 48 hoursafter surgery 2 At 72 hours after surgery 3 At 5 days after surgery 4 At 10 days after surgery 5 At 3 months after surgery

Countries

India

Contacts

Public ContactDr Nikash P John

Christian Medical College

pradeep.cmc@gmail.com8903310075

Outcome results

None listed

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