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Pain Intensity After Root Canal Instrumentation

A

Ain Shams University

Status

Completed

Conditions

Pain, Postoperative

Treatments

Device: mechanical preparation of root canal system

Study type

Interventional

Funder types

Other

Identifiers

NCT04216940
pain intensity

Details and patient eligibility

About

Assess the pain intensity in a two visit treatment of molars with irreversible pulpitis after instrumentation with two rotary systems Mpro and Hyflex files.

Enrollment

50 patients

Sex

All

Ages

25 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • mandibular molars with acute pulpitis

Exclusion criteria

  • badly decayed non-restorable molars
  • medically compromised patients

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

M-pro
Experimental group
Treatment:
Device: mechanical preparation of root canal system
Hyflex
Experimental group
Treatment:
Device: mechanical preparation of root canal system

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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