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

Effects of Polyvinylpyrrolidone Iodine Concentrations on Postoperative Trismus and Swelling Using as an Irrigation Solution During Impacted Third Molar Surgery : a Randomized Clinical Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03894722
Enrollment
80
Registered
2019-03-28
Start date
2016-10-03
Completion date
2018-02-09
Last updated
2019-03-28

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

Conditions

Impacted Third Molar Tooth

Keywords

third molar surgery, povidone iodine

Brief summary

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.

Interventions

PROCEDUREControl

During the third molar extraction the saline solution will be used in the control group.

PROCEDURE0.5% concentration of PVP-I

During the third molar extraction 0.5% concentration of PVP-I solution will be used in the test group.

PROCEDURE1 % concentration of PVP-I

During the third molar extraction 1 % concentration of PVP-I solution will be used in the test group.

PROCEDURE3 % concentration of PVP-I

During the third molar extraction 3 % concentration of PVP-I solution will be used in the test group.

Sponsors

Cansu Gül Koca
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative Facial Swelling (assessed 3 facial lines (in millimeters) for determination of difference in facial contours before and after surgery)Preoperative (on the day of surgery)- postoperative 2nd day-postoperative 7th dayFor the assessment of facial swelling, three facial lines (in milimeters) were measured with a digital tape on the operated side using following (4) landmarks: the external canthus of the eye, the gonion angle, the lower border of the tragus, soft pogonion and the mouth commissure Facial Lines between: 1. the external canthus of the eye- the gonion angle 2. the lower border of the tragus-the mouth commissure 3. the lower border of the tragus- soft pogonion
Postoperative Trismus (difference in interincisal distance at the maximal mouth opening (in millimeters) before and after surgery)Preoperative (on the day of surgery)- postoperative 2nd day-postoperative 7th day.The degree of trismus was assessed by measuring the distance between upper and lower incisal borders of the central incisors with a digital caliper.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026