Effectiveness of mannitol on postoperative complications after impacted mandibular third molar surgery

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20160712028892N2

Enrollment

Registered

2019-01-17

Start date

2019-02-01

Completion date

Unknown

Last updated

2019-01-29

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

Conditions

Correlation between complications associated with impacted mandibular third molar surgery and mannitol.

Interventions

Intervention 1: In this study, side of mandible in which mannitol is infused, is considered treatment group and would be selected randomly for each patient. Surgical removal of contralateral wisdom to

Eligibility

Sex/Gender

All

Age

16 Years to 64 Years

Inclusion criteria

Inclusion criteria: Taking no medications and drugs Healthy patients with ASA 1 category Lack of allergy to local anesthesia; Having bilateral mandibular third molar with similar impaction

Exclusion criteria

Exclusion criteria: Poor oral hygiene Smoking and alcohol abuse Pregnant and lactating mothers

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 1,2,4,6. Method of measurement: VAS scale.;Swelling. Timepoint: 2,4,6,8. Method of measurement: Sum of 3 distances: 1- Tragus to oral commisure; 2- Lateral canthus to Mandibular angle; 3- Tragus to Pogonion.;Trismus. Timepoint: 2,4,6,8. Method of measurement: Maximum opening measured between upper and lower incisors.	—

Secondary

Measure	Time frame
Patient satisfaction. Timepoint: 8. Method of measurement: Based on planned scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactOmid Soltaninia

Hamedan University of Medical Sciences

omid.soltaninia@umsha.ac.ir+98 81 3838 1059

Outcome results

None listed

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