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Comparing OHRQoL: One or Two Sessions for Wisdom Teeth Removal

Prospective Comparison of Single vs. Staged Extractions: OHRQoL Outcomes for Wisdom Teeth Removal

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05820867
Enrollment
59
Registered
2023-04-20
Start date
2018-03-01
Completion date
2021-09-01
Last updated
2023-04-20

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

Conditions

Impacted Third Molar Tooth, Impacted Tooth

Keywords

Quality of Life, Oral health, Prospective Studies, Molar, Third, Tooth Extraction, Patient Preference

Brief summary

This single-center prospective cohort study includes patients aged 18-30 years aimed to compare the effects of bilateral extraction of wisdom teeth at a single appointment (Group A) versus two separate appointments (Group B) on patients' oral health-related quality of life (OHRQoL). The primary outcome is Oral Health Impact Profile 14 score, while secondary outcomes included postoperative pain and maximum interincisal opening.

Interventions

PROCEDURESingle-Session Bilateral Mandibular Third Molar Extraction

Participants in this group chose to have both of their lower mandibular third molars extracted during a single appointment. This group will be used to compare the impact of single-session extraction on patients' oral health-related quality of life, postoperative pain, and maximum interincisal opening.

PROCEDURETwo-Session Bilateral Mandibular Third Molar Extraction

Participants in this group chose to have their lower mandibular third molars extracted during two separate appointments. This group will be used to compare the impact of two-session extraction on patients' oral health-related quality of life, postoperative pain, and maximum interincisal opening.

Sponsors

Marmara University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Patients referred to the Oral and Maxillofacial Surgery Department for bilateral extraction of impacted mandibular third molars. * Asymptomatic, impacted mandibular third molars. * Impaction classified as Class I, Position A according to the Pell and Gregory classification. * Patients with an ASA (American Society of Anesthesiologists) Physical Status Classification of ASA 1.

Exclusion criteria

* Local pathology associated with third molars (e.g., cysts or tumors). * Diagnosis of acute pericoronitis. * Usage of anti-inflammatory drugs or antibiotics within the last week. * Operations requiring osteotomy. * Patients with psychiatric disorders or taking drugs that may impair their mental health. * Patients unwilling to undergo data collection procedures. * Pregnant or lactating women. * Heavy smokers. * Operations lasting longer than 45 minutes for one side (from the time the first incision is made to the last suture placed).

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline oral health-related quality of life at 14 daysBaseline, postoperative day 2, day 3, day 7, day 9, and day 14The Oral Health Impact Profile-14 (OHIP-14) questionnaire is used to evaluate the participants' oral health-related quality of life. The OHIP-14 is a validated instrument that assesses the perceived impact of oral conditions on an individual's well-being across 14 items, each scored on a 5-point Likert scale. Lower scores indicate better OHRQoL.

Secondary

MeasureTime frameDescription
Change from baseline postoperative pain at 14 daysPostoperative 6th hour, 12th hour, day 2, day 3, day 7, day 9, and day 14The Visual Analog Scale (VAS) is used to assess the intensity of postoperative pain experienced by participants. The VAS is a validated tool consisting of a horizontal or vertical line, usually 100 mm in length, with anchor points of no pain at one end and worst imaginable pain at the other. Participants are asked to mark the point on the line that corresponds to their pain level. Higher scores indicate greater pain intensity.
Change in maximum interincisal openingBaseline and postoperative day 7Maximum interincisal opening (MIO) is being measured to evaluate trismus, or restricted mouth opening, following the extraction of mandibular third molars. MIO measurements are taken using a ruler to measure the distance between the upper and lower central incisors when the participant opens their mouth as wide as possible. Lower values indicate greater trismus.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026