CTRI/2020/02/023538
Not yet recruiting
Phase 4
Comparison of efficacy and safety of fentanyl transdermal patch with oral ketorolac for pain management in dry socket.
Department Oral health sciences centre0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: PCS- Health Condition 2: R52- Pain, unspecified
- Sponsor
- Department Oral health sciences centre
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility 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
- •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
Outcomes
Primary Outcomes
Not specified
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