Postoperative Course Following Wisdom Tooth Surgery

NCT00921479 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2021-11-05

No results posted yet for this study

Summary

The purpose of this study is to determine how quality of life changes after surgical removal of wisdom teeth

Conditions

  • Pain, Postoperative

Sponsors & Collaborators

  • University of Oslo

    collaborator OTHER
  • Ullevaal University Hospital

    lead OTHER

Principal Investigators

  • Lasse A Skoglund, DDS, DSci · Section of Dental Pharmacology and Pharmacotherapy, Faculty of Dentistry, University of Oslo

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-06-30
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00921479 on ClinicalTrials.gov