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A clinical trial to compare the safety and efficacy of transdermal fentanyl patch and oral ketrolac for pain management in dry socket patients.

Comparison of efficacy and safety of fentanyl transdermal patch with oral ketorolac for pain management in dry socket.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023538
Enrollment
60
Registered
2020-02-24
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: PCS- Health Condition 2: R52- Pain, unspecified

Interventions

Intervention1: TRANSDERMAL FENTANYL PATCH: Transdermal Fentanyl patch is one of the opioid analgesic that can be used for pain management for dry socket. Fentanyl, which is an opioid analgesic, was p

Sponsors

Department Oral health sciences centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients in the age group between 18- 60 years. 2. Patients who will return to the clinic with symptoms and signs of dry socket, including moderate to severe pain with a VAS score >4, will be included in this study. 3. Good physical and mental condition (ASA I ,II ) 4. Absence of infection or trauma. 5. Patients in which Zinc Oxide Eugenol (ZNOE) dressing is given. 6. Patients who can understand English and Hindi Languages.

Exclusion criteria

Exclusion criteria: 1. A history of allergy to the drugs used in the present study. 2. All pregnant and lactating females. 3. Alcohol or narcotics abusers. 4. Patients with ulcerative lesions or malignant lesions. 5. Patients who are taking monoamineoxidase inhibitor drugs. 6. Patients who are taking drugs for migraines. 7. Patients who are taking anti-retroviral, antifungal drugs. 8. Patient who have acute (sudden) or severe asthma. 9. Patient who has a gastrointestinal problem called paralytic ileus. 10. Heart or respiratory failure

Design outcomes

Primary

MeasureTime frame
1.PAIN SCORES IN DRY SOCKET Timepoint: 7 DAYS

Secondary

MeasureTime frame
1.SAFETY AND TOLERABILITY OF DRUGS. 2.NUMBER OF RESCUE MEDICATION TABLETS TAKENTimepoint: 7 DAYS

Countries

India

Contacts

Public ContactDr Abid Majeed Rather

PGIMER CHANDIGARH

drabidr8@gmail.com9872353508

Outcome results

None listed

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