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Effects of Polyvinylpyrrolidone Iodine on Postoperative Trismus and Swelling During Impacted Third Molar Surgery

C

Cansu Gül Koca

Status and phase

Completed
Phase 4

Conditions

Impacted Third Molar Tooth

Treatments

Procedure: Control
Procedure: 0.5% concentration of PVP-I
Procedure: 1 % concentration of PVP-I
Procedure: 3 % concentration of PVP-I

Study type

Interventional

Funder types

Other

Identifiers

NCT03894722
CHR: 2016-8/11

Details and patient eligibility

About

The aim of the present study was to evaluate the effects of different concentrations of povidone iodine (PVP-I) on postoperative swelling and trismus when used as a coolant and irrigation solution during the surgical removal of impacted mandibular third molars.

Enrollment

80 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Totally impacted mandibular third molars of class C, 1, 2, and 3 according to the Pell-Gregory classification;
  • Has no systemic disease

Exclusion criteria

  • The use of medications that could interfere with the healing process;
  • Smoking;
  • Pregnancy or lactation;
  • Presence of any condition, such as inflammation, periodontitis, gingivitis and dental abscess in the area of the impacted teeth;
  • Undergoing antibiotic or anti-inflammatory drugs therapies in the 7 days before surgery;
  • History of hypersensitivity to iodine;
  • Has any thyroid diseases.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

80 participants in 4 patient groups, including a placebo group

Group I (control; saline only)
Placebo Comparator group
Description:
Control Group: Intraoperative irrigation with saline solution only.
Treatment:
Procedure: Control
Group II (0.5% concentration of PVP-I )
Experimental group
Description:
Experimental Group: Intraoperative irrigation with 0.5% concentration of PVP-I solution.
Treatment:
Procedure: 0.5% concentration of PVP-I
Group III (1% concentration of PVP-I)
Experimental group
Description:
Experimental Group: Intraoperative irrigation with 1% concentration of PVP-I solution.
Treatment:
Procedure: 1 % concentration of PVP-I
Group IV (3% concentration of PVP-I)
Experimental group
Description:
Experimental Group: Intraoperative irrigation with 3% concentration of PVP-I solution.
Treatment:
Procedure: 3 % concentration of PVP-I

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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