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A Comparison between Continuous Femoral nerve block and Continuous Adductor canal block for Post operative pain relief in one sided Total knee replacement (TKR) surgeries.

Not yet recruiting
Conditions
Diseases of the musculoskeletal system and connective tissue, (2) ICD-10 Condition: M171||Unilateral primary osteoarthritisof knee,
Registration Number
CTRI/2023/05/052872
Lead Sponsor
Department of Anaesthesia Kokilaben Dhirubhai Ambani Hospital
Brief Summary

It is a  prospective,comparative study

Sample 

After routine pre-operative investigations and history, written

informed consent will be taken. The method of analgesia will be

decided by a computer generated list. On the day of

surgery, pain, nausea and vomiting will be assessed. The

physiotherapist will assess the muscle strength, pain at rest and post

physiotherapy at 24hrs and 48 hrs using our pre-designed case

record forms. Muscle strength will be assessed using Manual muscle

testing scale and pain using the VAS score

Total opiod requirement in 48hrs will be recorded.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
88
Inclusion Criteria
  • Age group: 18yrs and above All patients who would voluntarily agree to sign informed consent form.
  • All patients undergoing U/L Primary Total Knee Arthroplasty No contraindication to paracetamol, opioids and NSAIDS.
  • Spinal/General Anaesthesia Physical status ASA I and II.
Exclusion Criteria

Bilateral TKA at the same time Revision TKA Physical status ASA III and above.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the functional outcome of continuous femoral nervePain score at rest at 12hrs | pain score at rest and post exercise at 24hrs and 48hrs | nausea and vomiting at 12hrs, 24hrs and 48hrs | total fentanyl PCA requirement at 48hrs
block, continuous versus Adductor canal block in TKA patients and design aPain score at rest at 12hrs | pain score at rest and post exercise at 24hrs and 48hrs | nausea and vomiting at 12hrs, 24hrs and 48hrs | total fentanyl PCA requirement at 48hrs
clinical analgesic pathway.Pain score at rest at 12hrs | pain score at rest and post exercise at 24hrs and 48hrs | nausea and vomiting at 12hrs, 24hrs and 48hrs | total fentanyl PCA requirement at 48hrs
Secondary Outcome Measures
NameTimeMethod
Total opiod requirement of IV Fentanyl PCA postoperatively in48hrs in both groups of patients.

Trial Locations

Locations (1)

Kokilaben Dhirubhai Ambani Hospital

🇮🇳

(Suburban), MAHARASHTRA, India

Kokilaben Dhirubhai Ambani Hospital
🇮🇳(Suburban), MAHARASHTRA, India
Minoti Kamdar
Principal investigator
9702810568
minotikamdar@gmail.com

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