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Pre Emptive Analgesics for Pain Relief in Impacted Lower Third Molar Surgery

M

Melaka Manipal Medical College

Status and phase

Completed
Phase 4

Conditions

Impacted Third Molar Tooth

Treatments

Drug: Placebo
Drug: paracetamol

Study type

Interventional

Funder types

Other

Identifiers

NCT04769557
MMMC/FOD/AR/B5/E C-2017(07)

Details and patient eligibility

About

The purpose of the study is to evaluate the efficacy of pre-emptive paracetamol in reducing intra operative pressure and post operative pain after surgical removal of impacted mandibular third molar using visual analogue scale

Enrollment

60 patients

Sex

All

Ages

21+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients aged 21 years and above
  • Healthy patients (ASA I)
  • Patients who are not allergic to the drugs and local anesthetic agents used

Exclusion criteria

  • Patients who are on concurrent treatment with NSAIDs or corticosteroids
  • Patients with pericoronitis or periapical infection

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups, including a placebo group

Paracetamol
Experimental group
Description:
Paracetamol
Treatment:
Drug: paracetamol
Placebo
Placebo Comparator group
Description:
placebo
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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