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RecruitingNCT07765745Updated Aug 14, 2026

Effect of Thymoquinone 0.2% Gel on Bone Density, Bone Width, and Socket Preservation After Tooth Extraction

An interventional study of Gel foam and Thymoquinone gel + gel foam in Radiographic Evaluation, Bone Density and Bone Width, sponsored by Kafrelsheikh University. Recruiting at 1 site in Egypt. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-08-14.

Sponsored by Kafrelsheikh University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Feb 2026, registered Aug 2026).
  • Started Feb 2026; still recruiting 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

This study aims to evaluate the clinical and radiographic effects of 0.2% Thymoquinone gel on bone density, bone width, and socket preservation after tooth extraction.

Read the detailed description

Tooth extraction triggers a cascade of biological events which lead to significant remodeling of the alveolar ridge, frequently resulting in reductions in both bone width and height.

The concept of alveolar ridge preservation (ARP) has developed to address the bone resorption that follows extraction. ARP aims to maintain ridge dimensions and reduce the need for further augmentation before implant placement.

Among these, the small-molecule Thymoquinone (TQ), derived from Nigella sativa, has demonstrated significant osteogenic, anti-inflammatory, and antioxidant effects in preclinical studies.

02

Conditions studied

  • Radiographic Evaluation
  • Bone Density
  • Bone Width
  • Socket Preservation
  • Tooth Extraction
  • Thymoquinone
03

In context

Lead sponsor

Kafrelsheikh University is the lead sponsor of 294 studies on the registry; 114 are open to participants now.

Of its 10 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

04

Who can participate

Ages eligible
18 Years to 50 Years
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

  • Age: 18-50 years.
  • Both sexes.
  • Patients requiring extraction of upper posterior teeth will be recruited.

Exclusion criteria

Exclusion Criteria:

  • Healthy subjects with intact sockets after extraction.
  • Normal mouth opening and good oral hygiene.
  • No systemic conditions affecting bone healing.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Active comparator
    Group I (Negative Control)

    Patients will receive gel foam only

    Drug: Gel foam

  • Experimental
    Group II (Study Group 1)

    Patients will receive 0.2% thymoquinone gel + gel foam.

    Drug: Thymoquinone gel + gel foam

  • Experimental
    Group III (Study Group 2, Nano)

    Patients will receive nano-formulated 0.2% thymoquinone gel + gel foam.

    Drug: Nano-formulated 0.2% thymoquinone gel + gel foam

Interventions

  • DrugGel foam

    Patients will receive gel foam only.

  • DrugThymoquinone gel + gel foam

    Drug page: Thymoquinone

    Patients will receive 0.2% thymoquinone gel + gel foam.

  • DrugNano-formulated 0.2% thymoquinone gel + gel foam

    Patients will receive nano-formulated 0.2% thymoquinone gel + gel foam.

06

What researchers measure

Primary outcomes

  1. Change in alveolar bone density after tooth extraction

    Alveolar bone density will be assessed radiographically using cone-beam computed tomography (CBCT). The change in bone density from baseline to the specified postoperative assessment will be compared.

    Time frame: 3 months after tooth extraction

Secondary outcomes

  1. Change in alveolar bone width after tooth extraction

    Alveolar bone width will be assessed radiographically using cone-beam computed tomography (CBCT). The change in alveolar ridge width from baseline to the postoperative assessment will be measured.

    Time frame: 3 months after tooth extraction

  2. Change in alveolar ridge dimension after tooth extraction

    Alveolar ridge dimensions will be assessed radiographically using cone-beam computed tomography (CBCT). Changes in the dimensions of the alveolar ridge following tooth extraction will be measured and compared.

    Time frame: 3 months after tooth extraction

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes — The data will be available upon a reasonable request from the corresponding author after the end of study for one year.

Supporting information: Study protocol

Time frame: After the end of study for one year.

Access criteria: The data will be available upon a reasonable request from the corresponding author

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07765745
Responsible party
Muataz Adnan Karimeh (Oral and Maxillofacial Surgery, Faculty of Dentistry, Kafrelsheikh University, Kafrelsheikh, Egypt., Kafrelsheikh University) — Principal investigator
First posted
Aug 14, 2026
Start date
Feb 1, 2026
Primary completion
Feb 1, 2027 (estimated)
Completion
Feb 1, 2027 (estimated)
Last update
Aug 14, 2026

Study contacts

Muataz A Karimeh, Bachelor
Contact
moataz.karema1998@gmail.com
00201027988331

Oversight

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: Thymoquinone

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