ClinicalTrials.gg
Not yet recruitingNCT06452134Updated Jun 11, 2024

Evaluation the Effect of Coenzyme Q10 on Tissue Healing Process in Patients Undergoing Wisdom Tooth Extraction

A Phase 4 interventional study of Coenzyme Q10 100 MG Oral Tablet and Placebo in Molar, Third, Temporomandibular Joint Disorders and Dry Socket, sponsored by Zahra Nejati. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-06-11.

Sponsored by Zahra Nejati · Phase 4, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Sep 2024, 2 years 2 months ago, but the record still lists the study as not yet recruiting.
Phase
Phase 4
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to asses the effect of Coenzyme Q10 administration in patients from any gender group who are older than 18 years old undergoing wisdom tooth extraction. The main questions it aims to answer are:

does Coenzyme Q10 help with better tissue healing? does Coenzyme Q10 administration lower the prevalence of Dry socket after surgery? does Coenzyme Q10 prevent TMD (Temporomandibular disorders) while recovering from surgery? how does Coenzyme Q10 administration effect the answers to SF-36 health survey in patients? Researchers will compare Coenzyme Q10 to a placebo (a look-alike substance that contains no drug) to see if it has any effect on mentioned parameters.

Participants will:

  • take coenzyme Q10 (100mg) daily for 30 days after surgery.
  • will be examined and evaluated 1, 7, 14 and 30 days after completion of surgery.
02

Conditions studied

  • Molar, Third
  • Temporomandibular Joint Disorders
  • Dry Socket
  • Coenzyme Q10

Keywords

  • coenzyme Q10
  • Dry Socket
  • Temporomandibular Joint Disorders
  • Molar, Third
  • SF-36 health survey
  • Tissue healing
  • Tooth Extraction
  • GHQ-12
03

In context

Temporomandibular Joint Disorders

591 studies on the registry are indexed under Temporomandibular Joint Disorders; 149 are open to participants now.

This study's planned enrollment of 70 is above the median of 45 across 415 interventional studies indexed under Temporomandibular Joint Disorders.

Browse Temporomandibular Joint Disorders studies →

Lead sponsor

This is the only study on the registry with Zahra Nejati as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients older than 18 years old that require mandibular or maxillary molar, third tooth extraction as Oral and Maxillofacial surgeon's clinical diagnosis.

Exclusion criteria

Exclusion Criteria:

  • The patient's departure from Sanandaj
  • The patient's disagreement with the study protocol
  • The Patient's demise
  • The patient's hospitalization for unrelated illnesses
  • The patient's discontent with the care they received
  • The patient's failure to show up for follow-up appointments
  • The patient's sensitivity to Coenzyme Q10
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
70 participants (estimated)

Study arms

  • Experimental
    Intervention group

    This arm of the study includes 35 of participants who will be given Coenzyme Q10 100 MG Oral Tablet for 30 days.

    Drug: Coenzyme Q10 100 MG Oral Tablet

  • Placebo comparator
    Control group

    This arm of the study includes 35 of participants who will be given Placebo ( a look-alike substance ) with same tablet form given daily for a period of 30 days after surgery.

    Drug: Placebo

Interventions

  • Coenzyme Q10 oral Tablet with dosage of 100mg daily given for a period of 30 days after surgery.

    Also known as: Coenzyme Q, CoQ, CoQ10, Ubiquinone, Ubiquinone-Q10, Ubidecarenone, Vitamin Q10

  • DrugPlacebo

    Exactly same looking agent in the form of a tablet with same size and color to CoezymeQ10 with no active property given for a period of 30 days after surgery.

06

What researchers measure

Primary outcomes

  1. Rate of Tissue healing

    Regeneration-the replacement of damaged tissues with cells of the same type-and fibrosis-the replacement of damaged tissues with connective tissue-are the two primary processes involved in wound healing. To help in tissue healing, some cells, such as fibroblasts and vascular endothelial cells, have the ability to proliferate quickly in response to an external stimulation. Wound closure also requires non-proliferating cells, such as peripheral nervous system cells and odontoblasts. The bone that grows in to fill the space left by a tooth extraction should be similar to the surrounding healthy tissues. A lack of tissue healing is indicated by symptoms such as edema, fever, bleeding, discomfort, necrosis, exudate, flap instability, foul taste, and fistula. If trismus results from a muscle injury following an IAN Block injection, it should go away as the tissue heals.

    Time frame: 1, 7, 14 and 30 days after surgery

Secondary outcomes

  1. Incidence of Temporomandibular disorders

    Temporomandibular disorders is a collective term for a set of disorders characterized by pain and dysfunction in the muscles and jaw joint. A specialist dentist will measure a patient's temporomandibular disorder (TMD) clinically by looking for signs of trismus, abnormal movement of the lower jaw during opening and closing or chewing, jaw dysfunction, reduced range of motion, ear pain, temporal pain, headache, bruxism, sensitivity of the muscles in the neck and shoulders, and malocclusion (such as acquired edentulism, facial asymmetry, etc.). The diagnosis of TMD is finalized if the symptoms are positive.

    Time frame: 1, 7, 14 and 30 days after surgery

  2. Occurrence of Dry socket

    This is a non-scientific phrase for a cavity where all or part of the bone is exposed since there isn't any bone in the days following extraction. This can happen inside the cavity or outside the occlusal environment of the cavity. Severe recurrent pain results from the patient's inability to stop the mechanical stimulation of food particles or tongue on the exposed bone, which is extremely painful to touch. A specialized physician measures it by doing a clinical examination as well as by observing the whiteness of the bone-which is empty and uncomfortable to the touch-in the extracted tooth's socket.

    Time frame: 1, 7, 14 and 30 days after surgery

  3. Answers to The Short Form Health Survey-36

    This tool has shown to be useful in a variety of contexts, including clinical practice, the assessment of health policies, and general security investigations. The 36-item form was created in the United States in 1992 by Ware and associates, and studies on a range of patient populations have assessed its validity and reliability. This questionnaire's topics are not restricted to any one age range, illness, or condition. By adding the results of the eight health-forming categories, the questionnaire's design aims to assess the state of health from both a physical and mental standpoint. This survey, which consists of 63 items, rates eight distinct health domains using a scoring system derived from the table found in the reference. To score the SF-36, scales are standardized with a scoring algorithm or by the SF-36v2 scoring software to obtain a score ranging from 0 to 100. Higher scores indicate better health status.

    Time frame: 1, 7, 14 and 30 days after surgery

  4. Answers to The General Health Questionnaire-12

    Developed in the 1970s, the General Health Questionnaire (GHQ) is regarded as a valid and dependable instrument for evaluating mental health. The most popular of the various iterations of this survey is the GHQ-12 version. It is a 12-item mental health assessment that is assessed using the table given in the reference.The scores typically used are the binary scale (0-0-1-1) and the 4-point Likert-type scale (0-1-2-3). Responses to all items are summed up to a total score ranging from 0 to 12 (binary scale) or 0 to 36 (Likert scale), with higher scores indicating more severe impairment.

    Time frame: 1, 7, 14 and 30 days after surgery

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

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Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 11, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06452134
Lead sponsor
Zahra Nejati
Collaborators
Kurdistan University of Medical Sciences, Hady Mohammadi, Director of oral and maxillofacial surgery department, school of dentistry, Kurdistan university of medical sciences, Yousef Moradi, Assistant professor, Department of epidemiology and biostatistics, Kurdistan university of medical sciences, Babak Ghadirzadeh, medical student, Kurdistan university of medical sciences
Responsible party
Zahra Nejati (Zahra Nejati, Dental student, Department of oral and maxillofacial medicine, School of Dentistry, Kurdistan University of Medical Sciences, Sanandaj, Iran., Kurdistan University of Medical Sciences) — Sponsor-investigator
First posted
Jun 11, 2024
Start date
Jul 2024 (estimated)
Primary completion
Sep 2024 (estimated)
Completion
May 2025 (estimated)
Last update
Jun 11, 2024

Study contacts

Zahra Nejati
Contact
Znregina@gmail.com
+989220243892
Babak Ghadirzadeh
Contact
Ghadirzadeh.babak@gmail.com
+989355795670
Zahra Nejati
study director · Zahra Nejati, Department of oral and maxillofacial medicine, School of Dentistry, Kurdistan University of Medical Sciences, Sanandaj, Iran.

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Coenzyme Q10

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