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Effect of Preoperative Clindamycin on Postoperative Endodontic Pain

NCT03033472 · Status: UNKNOWN · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 72

Last updated 2017-01-27

No results posted yet for this study

Summary

The aim of this prospective, randomized, placebo controlled study is to evaluate the effect of clindamycin on post-operative pain and swelling in adult patient with symptomatic apical periodontitis.

Conditions

  • Symptomatic Periapical Periodontitis

Interventions

DRUG

600 mg Clindamycin orally

600 mg Clindamycin orally 30 minutes before treatment

DRUG

Oral Placebo

Oral Placebo 30 minutes before treatment

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Nermeen SA El Sedawy, Post Graduate · Cairo University

  • Suzan AW Wanees, PhD · Cairo Univertsity

  • Shaimaa Gawdat, PhD · Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Primary Completion
2017-12-31

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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 NCT03033472 on ClinicalTrials.gov