NCT05962593

Brief Summary

Removal of mandibular third molars (M3s) is the most frequently performed surgical intervention undertaken in dentistry. The indications and timing of surgical removal of M3s has been a matter of international and national debate, and especially prophylactic removal of M3s is controversial.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
124

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jun 2023

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2023

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

July 18, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 27, 2023

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2024

Completed
Last Updated

July 27, 2023

Status Verified

June 1, 2023

Enrollment Period

1 year

First QC Date

July 18, 2023

Last Update Submit

July 18, 2023

Conditions

Wisdom Teeth

Keywords

wisdom teethinflamationpain

Outcome Measures

Primary Outcomes (1)

  • Inflammation

    High sensitive C-reactive protein

    3 months postoperative

Secondary Outcomes (1)

  • Pain score

    1-7 days postoperative

Study Arms (2)

Telephone call

PLACEBO COMPARATOR

A postoperative telephone call

Other: Telephone call

No telephone call

NO INTERVENTION

No telephone call

Interventions

Telephone callOTHER

The patients will be randomized for a postoperative telephone call

Telephone call

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Wisdom teeth

You may not qualify if:

  • No wisdom teeth

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rigshospitalet

Copenhagen, 2100, Denmark

RECRUITING

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Marie Kj Larsen, PhD

    University of Copenhagen

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Marie Kjærgaard Larsen, PhD

CONTACT

+4520122781marie.kjaergaard@sund.ku.dk

Simon St Jensen, Prof

CONTACT

+4535 33 30 52simon.storgaard.jensen@sund.ku.dk

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
DIAGNOSTIC
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 18, 2023

First Posted

July 27, 2023

Study Start

June 1, 2023

Primary Completion

June 1, 2024

Study Completion

June 1, 2024

Last Updated

July 27, 2023

Record last verified: 2023-06

Locations

DK(1)