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Study of postoperative analgesia upon application of Transdermal Fentanyl patch after operation of knee replacement under spinal anaesthesia

Study of postoperative analgesia after preoperative application of Transdermal Fentanyl patch in cases operated for total knee replacement under spinal anaesthesia - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059984
Enrollment
40
Registered
2023-11-17
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Health Condition 1: M171- Unilateral primary osteoarthritisof knee Health Condition 2: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: Fentanyl patch 25 mcg /hr: Group F- Fentanyl patch 25 mcg/hr , transdermal route over anterior chest wall Intervention2: NO Fentanyl patch: Group C - Will Not receive transdermal patch

Sponsors

SHREE KRISHNA HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patient ASA (American society of anesthesiologist) 1-3 physical status 2) Patient undergoing total knee replacement surgery

Exclusion criteria

Exclusion criteria: 1) Absolute contraindication to spinal anaesthesia 2) Skin infection local site 3) Pregnancy 4) Allergy to local anaesthetic drug, TFP 5) Patient with pre-existing neurological deficit 6) Requirement of conversion to general anaesthesia due to inadequate block 7) Intolerance to or dependence on opioid 8) Known case of Severe obstructive or restrictive lung disease

Design outcomes

Primary

MeasureTime frame
To evaluate the post operative analgesia in patients who will undergone Total Knee Replacement (TKR) surgery with pre-operative use of transdermal fentanyl patchTimepoint: post operative period o-48 hour—

Secondary

MeasureTime frame
To assess NRS (Numeric Rating Scale) at rest and at movement of ankle joint and knee joint and in post operative Total Knee Replacement surgeries patients in both control and interventional (TFP group)Timepoint: 0 hours,2 hours, 4 hours,6 hours..... uoto 48 hours—

Countries

India

Contacts

Public ContactDr Krishna Malaviya

Pramukhswami Medical College,Bhaikaka University

malaviyakrishna3110@gmail.com9426216660

Outcome results

None listed

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