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Assessment of Post Operative Swelling Among Patients Following Extraction of Impacted Third Molars

Assessment of Post Operative Swelling Among Patients Following Extraction of Impacted Third Molars

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07655089
Acronym
APOSTM
Enrollment
116
Registered
2026-06-17
Start date
2026-07-05
Completion date
2026-08-05
Last updated
2026-06-17

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

Conditions

Post Operative Swelling

Keywords

Impacted Mandibular Third Molar, Swelling,, Oral Surgery

Brief summary

This randomized controlled trial aims to compare Ward's incision and Comma incision regarding postoperative swelling following extraction of impacted mandibular third molars. Secondary outcomes include pain and bleeding assessed 48 hours after surgery. The findings will help identify the incision technique associated with better postoperative outcomes

Interventions

PROCEDUREWard's Incision

Patients allocated to Group A will undergo extraction of impacted mandibular third molars using Ward's incision. Depending on the degree of impaction, a sulcular incision will be made from the mesiobuccal aspect of the first or second molar extending distally. A relieving incision will be placed mesially without severing the interdental papilla, followed by a distal releasing incision on the mandibular ramus. A full-thickness mucoperiosteal flap will then be elevated to facilitate tooth extraction.

PROCEDUREComma Incision

Patients allocated to Group B will undergo extraction of impacted mandibular third molars using the Comma incision technique. The incision will begin below the second molar and extend to its distobuccal line angle, then curve smoothly upward to the gingival crest. The incision will continue as a crevicular incision around the distal aspect of the second molar. A distolingually based flap will be elevated to provide adequate exposure for extraction of the impacted third molar.

Sponsors

College of Physicians and Surgeons Pakistan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Patients aged 18-50 years. Male and female patients. Patients undergoing extraction of impacted mandibular third molars irrespective of angulation as evaluated radiographically. Patients with no periodontal pathology related to the involved tooth on clinical examination. \-

Exclusion criteria

* Patients with congenital or acquired bleeding disorders. Patients with any bony lesion adjacent to the impacted third molar. Medically immunocompromised patients.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative Swelling48 hours after surgeryDegree of postoperative swelling assessed using a Visual Analog Scale (VAS) ranging from 0 to 5, where 0 indicates no swelling and 5 indicates extremely severe swelling following extraction of impacted mandibular third molars

Contacts

CONTACTFatima Khattak Khattak
fatimakhattak32@gmail.com03315125534

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 18, 2026