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Completed

NCT Number: NCT06918327

Effect of CGF on Postoperative Pain After Third Molar Surgery

The purpose of this study is to evaluate the effects of concentrated growth factor (CGF) on pain after bilateral impacted third molar surgery and to determine its contribution to the healing process.

The main question it aims to answer is:

Is CGF effective on reducing the pain in impacted third molar surgery? Researchers compare the pain on the CGF-applied and CGF free sides after impacted third molar surgery. Postoperative pain is assessed using the Visual Analogue Scale. TThe postoperative outcomes including pain are clinically assessed at different-time intervals (1-7 days).

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ege University Faculty of Dentistry

Izmir, Bornova, 35040, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with bilateral, symmetrical, bone-retained (vertical, mesioangular, horizontal) impacted wisdom teeth in the mandible, regardless of gender
  • Patients without any systemic disease
  • Patients who have been informed about the duration, purpose and requirements of the study and who have signed the informed consent form voluntarily.

Exclusion criteria

  • Having a disease affecting general health that requires the application of prophylactic antimicrobial agents
  • Having a systemic viral, fungal or bacterial infection
  • Patients with acute or chronic maxillary sinusitis
  • Suspected or diagnosed pregnancy and nursing mothers
  • Patients with heart and vascular diseases
  • Patients with liver disease, haematological disease and neoplastic disease
  • Patients who have recently received anti-inflammatory therapy
  • Patients with chronic medication use (antihistamines, NSAIDs, steroids and antidepressants)
  • Patients predisposed to psychotic or psychopathic tendencies
  • Patients with rheumatic diseases, blood diseases, diabetes mellitus
  • Patients at cardiological risk of infective endocarditis
  • Patients under antibiotic pressure

Treatment and study plan

Concentrated Growth Factor

Other

Bilaterally impacted third molar of the patients are removed surgically and concentrated growth factor is placed in one of the extraction sockets.

non-CGF

Other

The other extraction socket is left empty for control purposes.

Primary outcomes

  1. Postoperative pain on CGF-applied and CGF free sides in bilateral impacted third molar surgery

    Time frame: The postoperative outcomes including pain are clinically assessed at different-time intervals (1st, 2nd, 3rd, 4th, 5th, 6th and 7th days).

    The primary outcome measure is postoperative pain on CGF-applied and CGF free sides in bilateral impacted third molar surgery. Postoperative pain is assessed using the Visual Analogue Scale (VAS). Patients are asked to mark the pain they felt on the scale (10 cm long line) on the (1-7) days after the operation. The end of the line indicates unbearable pain, the beginning indicates no pain.

Sponsors and collaborators

Lead sponsor

Ege University

Other

Registry information

Official study title

The Power of Concentrated Growth Factor: A New Era in Pain Management in Third Molar Surgery

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Apr 9, 2025
Registry last updated
Apr 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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