Manufacturing of a topical dressing paste for treatment of alveolar osteitis

Phase 3

• Conditions: Dry socket.; Alveolitis of jaws; M27.3

• Registration Number: IRCT20200706048029N1
• 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: 7 September 2020

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Patients who seek treatment for dry socket due to dental extraction in Mashhad Dental school

Exclusion Criteria

Patient with a history of allergies to drugs or food
Patient do not refer for follow-up

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Measurement of patients' pain upon arrival (by VAS) and evaluation of pain intensity after application of any type of dressing. Timepoint: Measurement of pain upon arrival, at 30, 60 minutes, 24 hours and 48 hours after application until the patient is in pain continues daily. Method of measurement: Measurement of pain by using Visual Analog Scaling.;Check the number of times the dressing is used. Timepoint: Record the number of times the dressing is applied. Method of measurement: Record the number of times the dressing is applied.;Number of painkillers consumed during treatment. Timepoint: Number of painkillers consumed during treatment. Method of measurement: Record the number of painkillers used.