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Gelofen in wisdom tooth surgery

The effect of locally applied gelofen in postoperative complication after wisdom tooth surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181215041988N1
Enrollment
34
Registered
2019-07-11
Start date
2019-06-08
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Wisdom surgery. Dental drugs, topically applied

Interventions

Intervention 1: The intervention group is treated with gelofen-containing gelfoam in the socket of wisdom teeth. The contents of a 400 mg gelofen tablet (Jaber-ibne Hayan Co., Iran) is discharged by a

Sponsors

Ardabil University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 65 Years

Inclusion criteria

Inclusion criteria: Having an impacted mandibular wisdom tooth Age between 14 and 65 years Signature of consent

Exclusion criteria

Exclusion criteria: Systemic disease Pregnancy Drug abuse Using anti_ analgesic grug

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 2,4,6,12,24,48 hours after surgery. Method of measurement: visual analogue scale.

Secondary

MeasureTime frame
Bleeding. Timepoint: 2 days after surgery. Method of measurement: questionnaire.;Swelling. Timepoint: 2 days after surgery. Method of measurement: Measured by ruler from comissure of lip_ lop of ear and countus of eye _ Angle of mandible.;Trismus. Timepoint: 2 days after surgery. Method of measurement: distance between the upper and lower incisal edges in millimeters.;Dry sucket. Timepoint: 2 days after surgery. Method of measurement: Examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPouyan Sigari

Ardabil University of Medical Sciences

P.Sigari@arums.ac.ir+98 21 4454 1504

Outcome results

None listed

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