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Comparison of Conventional and Audiovisual Information on Anxiety and Postoperative Morbidity Following Third Molar Surgery: A Randomised Study.

Comparison of Conventional and Audiovisual Information on Anxiety and Postoperative Morbidity Following Third Molar Surgery: A Randomised Study.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201904716891248
Enrollment
90
Registered
2019-04-18
Start date
2019-03-25
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Oral Health

Interventions

verbal and audiovisual information

Sponsors

Obafemi Awolowo University Teaching Hospital Complex
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Participants aged between 18 years and 35 years. 2. Participants who have never had a tooth extraction. 3. Participants with impacted mandibular third molar confirmed by periapical radiograph and indicated for surgical extraction. 4. Participants who can understand and comprehend both written and verbal information about third molar extraction procedure. 5. Participants with complete maxillary and mandibular incisors to enable measurement of maximal inter-incisal distance 6. Participants who give consent to take part in the study.

Exclusion criteria

Exclusion criteria: 1. Participants with uncontrolled medical or systemic disease contraindicating surgical extraction under local anesthesia e.g. compromised cardiac function, hematological abnormalities, metabolic disorders, central nervous system disorder, impaired renal or hepatic function or depressed respiratory functions 2. Participants with chronic health conditions that affect blood pressure, pulse rate and heart rate such as sleep disorders. 3. Participants taking anxiolytic medications or receiving anxiety reduction therapy. 4. Participants with stress and anxiety disorders such as post-traumatic stress disorders assessed using trauma screening questionnaire. 5. Participants with peptic ulcer disease.

Design outcomes

Primary

MeasureTime frame
Pain Swelling Trismus

Secondary

MeasureTime frame
STAI-S MDAS

Countries

Nigeria

Contacts

Public ContactAyodele Akomolafe

Senior Registrar

drkomoo80@gmail.com+2347086270621

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026