comparison of efficacy of tramadol hydrochloride versus linocaine hydrochloride as Local anesthetic and analgesic agent A single blind split mouth study.
Phase 3
- Conditions
- Health Condition 1: K088- Other specified disorders of teethand supporting structures
- Registration Number
- CTRI/2024/06/069607
- Lead Sponsor
- DR SHUBHAM DILIP PHADTARE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Healthy Patients within age group 12 to 40 years.
2.Patients classified under ASA I.
3.Patients who are willing to participate in the study by signing the informed
consent.
4.Patients indicated for orthodontic extraction of maxillary premolar.
5.Patients who can comprehend the pain scale used in the study.
Exclusion Criteria
1.Patients classified under ASA II, III and IV.
2.Pregnant or lactating women.
3.Patients with previous history of allergy to Local Anaesthetic Agent.
4.Patients with previous history of allergy to tramadol.
5.Patients with pre-existing paresthesia.
6.Patients on antidepressants, anticoagulants, psychotropic drugs.
7.Epileptic Patients.
8.Patients under the Influence of Alcohol.
9.Patients requiring additional Anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method