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CompletedNCT07758192Updated Aug 11, 2026

Oral Flap Outline and Local Blood Supply After Surgical Removal of Lower Third Molar Teeth

An interventional study of Sulcular flap elevation for wisdom tooth removal and Three-cornered flap elevation for wisdom tooth removal in Surgical Flaps, Oral Surgical Procedures and Regional Blood Flow, sponsored by Betül Taş Özyurtseven. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-08-11.

Sponsored by Betül Taş Özyurtseven · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 5 years 8 months after the study started (first participant enrolled Nov 2020, registered Aug 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
56
Allocation
Non-randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

Wisdom teeth in the lower jaw are frequently buried in bone and must be taken out surgically. To reach the tooth, the surgeon lifts the gum away from the bone as a flap, and the shape of that flap is left to the surgeon's judgement. Two outlines are in everyday use. The first runs only along the necks of the teeth, so the gum is lifted without any additional cut. The second adds a short downward cut in front, which opens the field more widely but also divides some of the small vessels that run within the gum.

Because the tissues around a wound rely on a rich network of tiny vessels while they repair themselves, it is worth knowing whether these two outlines leave the local circulation in a different state. This project measured that circulation directly. A laser probe was placed against the tooth in front of the extraction site and against three points on the cheek-side gum, and the amount of moving blood beneath the probe was recorded. To make sure the probe returned to exactly the same spots at every visit, a thin clear plastic guide with prepared openings was made for each participant from a plaster model of the mouth.

Measurements were taken before the operation and again on the third and the seventh day afterwards. Facial swelling and how widely the mouth could be opened were recorded on the same occasions. Participants were assigned to one of the two flap outlines in turn, and every operation was carried out by the same surgeon so that the comparison depended on the flap outline alone.

Read the detailed description

Fifty-six systemically healthy adults presenting for surgical removal of a single fully bone-impacted mandibular wisdom tooth were assigned to one of two mucoperiosteal flap outlines by an alternating (non-random) sequence, giving twenty-eight participants per arm. Assignment was stratified by angulation according to Winter's scheme, so that each of the four angulation categories contributed seven cases to each arm.

Microvascular perfusion was quantified in perfusion units using a laser Doppler flowmeter (Perimed, Järfälla, Sweden). One recording site lay on the mid-buccal aspect of the tooth immediately anterior to the extraction site, at the crossing of its mesiodistal and occlusocervical axes, and served as an index of pulp circulation; three further sites were distributed over the adjacent buccal mucosa. Probe position was reproduced across visits by a 2 mm transparent acrylic stent carrying prepared probe housings, constructed individually on a stone model. Each site was sampled for 30 seconds.

Swelling was derived from three facial reference distances (gonion to labial commissure, tragus to labial commissure, and gonion to lateral canthus), averaged to a single value. Mouth opening was taken as the greatest interincisal distance. Every assessment was carried out immediately before surgery and repeated on the third and seventh postoperative days, sutures being removed at the final visit.

All operations were performed by one operator with a standard armamentarium under inferior alveolar, lingual and buccal block anaesthesia, using no more than two cartridges of articaine 40 mg/mL with epinephrine 1:100,000. Bone was removed and the tooth divided with a physiodispenser and steel burs under saline cooling, and the socket was closed with 3/0 silk. All participants received amoxicillin-clavulanate, paracetamol and a benzydamine-chlorhexidine mouthrinse after the procedure. Group means were compared by repeated-measures analysis of variance with Tukey HSD pairwise testing.

02

Conditions studied

  • Surgical Flaps
  • Oral Surgical Procedures
  • Regional Blood Flow
  • Tooth, Impacted
  • Molar, Third

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Keywords

  • mouth opening
  • swelling
  • mucosal perfusion
  • pulp circulation
  • laser Doppler flowmetry
  • vertical releasing incision
  • mucoperiosteal flap
  • impacted wisdom tooth
03

In context

Tooth, Impacted

122 studies on the registry are indexed under Tooth, Impacted; 15 are open to participants now.

This study's enrollment of 56 is below the median of 70 across 88 interventional studies indexed under Tooth, Impacted.

Browse Tooth, Impacted studies →

Lead sponsor

This is the only study on the registry with Betül Taş Özyurtseven as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Free of systemic illness and taking no regular medication
  • Aged 18 to 40 years
  • One fully bone-impacted mandibular wisdom tooth for which surgical removal is indicated
  • Ramus relationship of class II or III and depth position A, B or C on the Pell and Gregory scheme
  • Angulation falling into one of four categories on Winter's scheme: vertical, mesioangular, horizontal or distoangular
  • Neighbouring second molar intact, i.e. without extensive caries, endodontic treatment, a large filling or a crown
  • Willing and able to give written consent and to attend both follow-up visits

Exclusion criteria

Exclusion Criteria:

  • Any systemic disorder, or use of medication on a continuing basis
  • Tobacco use
  • Previous irradiation or chemotherapy involving the head and neck
  • Infection within the mouth at the time of surgery, including acute pericoronitis
  • Pregnancy or suspected pregnancy
  • Menstruation at the time of a scheduled measurement
  • Need for more than two anaesthetic cartridges to achieve profound anaesthesia
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
56 participants (actual)

Study arms

  • Active comparator
    Sulcular (envelope) flap

    The mucoperiosteum is raised through an incision confined to the gingival sulcus, carried from the mesial aspect of the first molar back to the distal aspect of the second molar and then along the external oblique ridge. No vertical cut is made.

    Procedure: Sulcular flap elevation for wisdom tooth removal

  • Active comparator
    Three-cornered (trapezoidal) flap

    The same sulcular and posterior incision is used, with the addition of a vertical relieving cut placed anterior to the second molar and kept clear of the interdental papilla.

    Procedure: Three-cornered flap elevation for wisdom tooth removal

Interventions

  • ProcedureSulcular flap elevation for wisdom tooth removal

    The mucoperiosteum is raised through an incision confined to the gingival sulcus, carried from the mesial aspect of the first molar back to the distal aspect of the second molar and then along the external oblique ridge.

    Also known as: Intervention 1

  • ProcedureThree-cornered flap elevation for wisdom tooth removal

    The same sulcular and posterior incision is used, with the addition of a vertical relieving cut placed anterior to the second molar and kept clear of the interdental papilla

06

What researchers measure

Primary outcomes

  1. Change in mucosal microcirculation adjacent to the operative field

    Perfusion in perfusion units (PU) at three buccal mucosal sites recorded by laser Doppler flowmetry through the same stabilising stent, 30 seconds per site. The most anterior site lies in the region traversed by the vertical relieving cut of the three-cornered outline.

    Time frame: Immediately before surgery, and on postoperative days 3 and 7

  2. Change in pulp microcirculation of the tooth adjacent to the extraction site

    Perfusion recorded in perfusion units (PU) by laser Doppler flowmetry over the mid-buccal aspect of the neighbouring second molar, with probe position reproduced by an individually made acrylic stent. Each recording lasts 30 seconds. A higher value indicates greater circulation.

    Time frame: Immediately before surgery, and on postoperative days 3 and 7

Secondary outcomes

  1. Change in facial swelling

    Mean of three facial reference distances measured in centimetres: gonion to labial commissure, tragus to labial commissure, and gonion to lateral canthus. A higher value indicates more swelling.

    Time frame: Immediately before surgery, and on postoperative days 3 and 7

  2. Change in maximum mouth opening

    Greatest interincisal distance in millimetres, used as an index of restricted opening. A lower value indicates greater restriction.

    Time frame: Immediately before surgery, and on postoperative days 3 and 7

  3. Duration of the operation

    Elapsed time in minutes from the first cut to placement of the final suture.

    Time frame: Day of surgery (day 0), intraoperative

07

Study locations

1 site
  • Gaziantep University, Faculty of Dentistry, Department of Oral and Maxillofacial Surgery
    Gaziantep, Gaziantep 27310, Turkey (Türkiye)
08

References and documents

Publications

  • Kirk DG, Liston PN, Tong DC, Love RM. Influence of two different flap designs on incidence of pain, swelling, trismus, and alveolar osteitis in the week following third molar surgery. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007 Jul;104(1):e1-6. doi: 10.1016/j.tripleo.2007.01.032. Epub 2007 May 15. PubMed 17507264 ↗

Individual participant data

Plan to share: No — available from the corresponding author on reasonable request

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07758192
Lead sponsor
Betül Taş Özyurtseven
Responsible party
Betül Taş Özyurtseven (Associate Professor of Oral and Maxillofacial Surgery, Senior Researcher / Clinician, University of Gaziantep) — Sponsor-investigator
First posted
Aug 11, 2026
Start date
Nov 9, 2020
Primary completion
Nov 9, 2021
Completion
Nov 9, 2021
Last update
Aug 11, 2026

Study contacts

Betül Taş Özyurtseven, DDS, PhD, Assoc. Prof. Dr.
principal investigator · University of Gaziantep

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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