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Evaluation of the Effect of Saffron (Crocus Sativus) on Pain Control After Root Canal Therapy in Teeth With Vital Pulps

NCT01590485 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2013-01-29

No results posted yet for this study

Summary

The purpose of this study is to determine whether saffron is effective in the pain control after root canal therapy in vital teeth.

Conditions

  • Post-treatment Pain Following Root Canal Therapy

Interventions

OTHER

starch

100 mg in each capsule every 6 hours up to 48 hours (400 mg/day)

OTHER

saffron

100 mg in each capsule every 6 hours up to 48 hours (400 mg/day)

Sponsors & Collaborators

  • Zahedan University of Medical Sciences

    lead OTHER

Principal Investigators

  • Kaveh Oloomi, DDS, MS · Zahedan University of Medical Sciences

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-05-31
Primary Completion
2013-01-31
Completion
2013-01-31

Countries

  • Iran

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01590485 on ClinicalTrials.gov