Effect of serum on the complications of third Molar surgery

Investigating the effect of the amount of serum used on the complications after third Molar surgery

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20191127045516N3

Enrollment

300

Registered

2021-01-02

Start date

2020-12-21

Completion date

Unknown

Last updated

2021-02-22

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

Conditions

Mandibular third molar surgery. Supernumerary teeth

Interventions

Intervention 1: Intervention group: Patients will receive 20 ml of normal sterile saline 5 minutes after surgery. The size of the syringe used for rinsing with serum is 20 ml. Intervention 2: Interven

Eligibility

Sex/Gender

All

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patients undergoing mandibular third molar surgery They should be in the moderate surgical group. The existence of a third mandibular molar, the occlusion of which has been confirmed by panoramic radiography.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: Immediately, 2 and 7 days after surgery. Method of measurement: Visual Analogue Scale (VAS).;Inflation. Timepoint: Immediately, 2 and 7 days after surgery. Method of measurement: self report.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamed Nazari

Kermanshah University of Medical Sciences

Nazari.hamed67@gmail.com+98 83 3722 7151

Outcome results

None listed

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