The effectiveness of curcumin in pain reduction in orthodontic patient

Phase 2

• Conditions: Orthodontic.; Fitting and adjustment of ileostomy and other intestinal appliances; Z46.5

• Registration Number: IRCT20200609047705N1
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 15 June 2020

Recruitment & Eligibility

• Status: Pending
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Female with aged range 14-30 years
No history of systemic disease
Nonuse of analgesic

Exclusion Criteria

Having a special medical condition
Having drug intolerance
Having gastrointestinal disorders

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The pain rate in chewing. Timepoint: 2, 6 hours, and 2 days after the intervention. Method of measurement: Visual Analogue Scale (VAS).;The pain rate in biting. Timepoint: 2, 6 hours, and 2 days after the intervention. Method of measurement: Visual Analogue Scale (VAS).;The pain rate in tipping anterior teeth. Timepoint: 2, 6 hours, and 2 days after the intervention. Method of measurement: Visual Analogue Scale (VAS).;The pain rate in put posterior teeth on each other. Timepoint: 2, 6 hours, and 2 days after the intervention. Method of measurement: Visual Analogue Scale (VAS).