Comparison of the effectiveness of Gelatamp and Hemospon on pain after impacted mandibular third molar surgery

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20210813052163N1

Enrollment

Registered

2021-09-06

Start date

2021-09-22

Completion date

Unknown

Last updated

2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

surgery of the impacted mandibular third molar. Impacted teeth

Interventions

Intervention 1: Intervention group is a group in which Gelatamp analgesic is used in their dental socket in a random method.first,each of the third molars is anesthetized by the surgeon by injecting t

Eligibility

Sex/Gender

All

Age

17 Years to 35 Years

Inclusion criteria

Inclusion criteria: study participants must be in the age range of 17 to 35. participants must have two impacted mandibular third molar teeth with the same latency conditions.(the occlusion on both sides must be mesioangular or vertical.)

Exclusion criteria

Exclusion criteria: the occlusion of the impacted mandibular third molar should not be distoangular or horizontal. existence of the acute or chronic inflammation of the coronary artery Taking drugs other than the drugs considered in the study failure to complete or submit the questionnaire Having systemic problems pregnancy Contraindications to the use of the drug used for the patient Having a neurological disease people taking steroids,antidepressants,antibiotics,analgesics The presence of painful conditions in the mouth such as teeth with indication for endodontic treatment Having any painful conditions in the body

Design outcomes

Primary

Measure	Time frame
Primary outcome variable:The amount of pain in questionnaire two. Timepoint: Measurement the amount of pain afeter surgery,after anesthesia,12 hours after surgery,1 day after surgery,2 days after surgery,3 days after surgery. Method of measurement: In this study ,the pain score after impacted mandibular third molar surgery in both groups is determined by using verbal pain criteria(0 to 10 score).;Secondry outcome variable: number of volatile analgesics used. Timepoint: The number of volatile drugs used by the patient is measured during the period between the end of anesthesia and three days after surgery. Method of measurement: The number of volatile analgesics used by the patient is measured by using questionnaire two provided to the patient.	—

Measure

Time frame

Primary outcome variable:The amount of pain in questionnaire two. Timepoint: Measurement the amount of pain afeter surgery,after anesthesia,12 hours after surgery,1 day after surgery,2 days after surgery,3 days after surgery. Method of measurement: In this study ,the pain score after impacted mandibular third molar surgery in both groups is determined by using verbal pain criteria(0 to 10 score).;Secondry outcome variable: number of volatile analgesics used. Timepoint: The number of volatile drugs used by the patient is measured during the period between the end of anesthesia and three days after surgery. Method of measurement: The number of volatile analgesics used by the patient is measured by using questionnaire two provided to the patient.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLasemi,Eshagh

Islamic Azad University

elasemi@yahoo.com+98 21 2256 4571

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026