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Use of buprenorphine patch for pain relief after heart surgery in adults

Efficacy of Transdermal Buprenorphine Patch in Post Operative Pain Management in Adult Cardiac Surgery - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112948
Enrollment
100
Registered
2026-06-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: - Health Condition 2: G891- Acute pain, not elsewhere classified

Interventions

Intervention1: Transdermal Buprenorphine Patch: Transdermal buprenorphine patch applied preoperatively for postoperative analgesia in adult patients undergoing elective cardiac surgery under general a

Sponsors

CAREER INSTITUE OF MEDICAL SCIENCES AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients aged 18 to 75 years Patients undergoing elective cardiac surgery under general anaesthesia ASA physical status 2 and 3 Patients willing to provide informed written consent

Exclusion criteria

Exclusion criteria: Known allergy to buprenorphine or opioids Severe hepatic or renal dysfunction Chronic opioid use or opioid dependence Patients with psychiatric illness or inability to understand pain scoring Emergency cardiac surgery Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
Postoperative pain intensity measured using Visual Analog Scale in adult patients undergoing cardiac surgery receiving transdermal buprenorphine patch.Timepoint: At 2 hours 6 hours 12 hours 24 hours and 48 hours after surgery

Secondary

MeasureTime frame
Secondary outcomes will include total rescue analgesic consumption during the first 72 hours after surgery, incidence of opioid-related adverse effects such as nausea, vomiting, sedation and respiratory depression, changes in hemodynamic parameters (heart rate and mean arterial pressure), and overall patient satisfaction with postoperative pain relief, which will be assessed during the first 72 hours following surgeryTimepoint: 24 h, 48 h, 72 h post-operativel

Countries

India

Contacts

Public ContactSHAIK ABDUL SALAM

CAREER INSTITUTE OF MEDICAL SCIENCES AND HOSPITAL

drgsrikanthdm@gmail.com9848477775

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026