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Evaluation the effect of iodine tampon usage on pain after wisdom tooth surgery

Evaluation the effect of iodine tampon usage on pain after partially-impacted mandibular third molar surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231221060486N1
Enrollment
35
Registered
2024-02-06
Start date
2024-02-19
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Partially-impacted mandibular third molar.

Interventions

Intervention 1: Intervention group: After tooth extraction, iodine tampon and then a gauze on it will be placed in the surgical site. Intervention 2: Control group: Gauze impregnated with physiologica

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Mesioangular bilateral partially-impacted mandibular third molar The patient should be placed in the systemic classification of class 1. The patient should be between 18 to 30 years old.

Exclusion criteria

Exclusion criteria: The patient's allergy to ibuprofen The patient's allergy to iodine Smoking and tobacco usage Presence of systemic disease Presence of acute perichronitis Presence of periodontal disease The patient recently or currently has a stomach ulcer The patient receives anticoagulation treatment Pregnancy or breastfeeding of the patient The patient has a history of local infection before surgery in the last 15 days History of radiotherapy in the jaw and face area Pathological disease related to the third molar

Design outcomes

Primary

MeasureTime frame
Pain score in visual analog scale (VAS) pain assessment. Timepoint: Pain score during the first week after surgery. Method of measurement: Visual analog scale (VAS) pain assessment.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirarsalan Yazdani Boroujeni

Islamic Azad University

arsalan.yazdani1378@gmail.com+98 21 8802 6163

Outcome results

None listed

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