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The Assessment of Curcuma Longa Potentials for Soft and Hard Tissue Healing in Fresh

The Assessment of Curcuma Longa Potentials for Soft and Hard Tissue Healing in Fresh Extraction Sockets; Randomized Controlled Clinical Trial.

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05816707
Enrollment
30
Registered
2023-04-18
Start date
2024-05-01
Completion date
2026-03-01
Last updated
2026-03-27

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

Conditions

Tooth Extraction Status Nos, Tooth Fracture

Brief summary

The study will be conducted on 30 patients with split mouth design patients will be divided into curcumin and PRF groups patients will have bilateral tooth extraction one side will receive curcumin/PRF and the other side will be control soft tissue healing and bone quality will be evaluated post-operative

Detailed description

30 Patients will be collected from the outpatient clinic of the Department of Oral &Maxillofacial surgery, Faculty of Dentistry, MSA University, Cairo, Egypt Eligibility criteria: Inclusion Criteria for participants: 1. Patients with bilateral badly decayed mandibular posterior tooth that need extraction. 2. Patients free from any systemic disease 3. Patients who approved to be included in the trial and signed the informed consent. 4. Patients with no signs or symptoms of acute periapical\\ periodontal infection. 5. Adults aged between 18-50 years old. Exclusion criteria for participants: 1. Patients who are allergic to Curcumin 2. Smoker patient 3. Patients receiving chemotherapy or radiotherapy. 4. Patients who refused to be included in the trial. Interventions: 1. Diagnosis * All patients will be diagnosed and selected according to inclusion and exclusion criteria. * Comprehensive clinical examination and understanding of patient's chief complains and needs will be done. * Standard preoperative intra-oral photographs (occlusal and lateral) * (Pre-operative orthopantogram\* will be taken to ensure absence of any periapical infection) 2. Intra-operative procedures: Local anesthesia\* will be injected intraoral around selected teeth. Patients will rinse by antiseptic mouthwash\*\* 30 seconds before extraction. Teeth will be extracted a-traumatically as possible to avoid any soft tissue or bony damage. The extracted sockets will be debrided by bone curettes and saline. The three extraction sockets will be divided into three groups: control group, curcumin group, and PRF group. After curcumin/ PRF placement, all sockets will be closed by simple interrupted suture\*\*\* 3. Postoperative treatment Analgesics \*\*\*\* every 6 hours for 3 days 4. Concomitant care None needed. 5. Follow up & Evaluation. * The extraction site will be inspected clinically after 3 days for signs of infection. * Soft tissue healing and pain score will be assessed after 7, 14, and 21 days. * 3 months post-operatively, each patient will undergo radiographic assessment by using Cone Beam Computed Tomography\*\*\*\*\*\* (CBCT) to evaluate bone healing and bone density.

Interventions

BIOLOGICALPRF

Teeth will be extracted a-traumatically as possible to avoid any soft tissue or bony damage. The extracted sockets will be debrided by bone curettes and saline. The three extraction sockets will be divided into three groups: control group, curcumin group, and PRF group. After curcumin/ PRF placement, all sockets will be closed by simple interrupted suture

BIOLOGICALCurcuma Longa gel

Curcuma Longa gel

OTHERextraction socket

extraction socket

Sponsors

Rania Farouk Mohamed Abdulmaguid
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

Randomized controlled clinical trial.

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* 1\. Patients with bilateral badly decayed mandibular posterior tooth that need extraction. 2\. Patients free from any systemic disease 3. Patients who approved to be included in the trial and signed the informed consent. 4\. Patients with no signs or symptoms of acute periapical\\ periodontal infection. 5\. Adults aged between 18-50 years old.

Exclusion criteria

* 1\. Patients who are allergic to Curcumin 2. Smoker patient 3. Patients receiving chemotherapy or radiotherapy. 4. Patients who refused to be included in the trial.

Design outcomes

Primary

MeasureTime frameDescription
Soft tissue healing21 days after surgeryHealing index (change is being assessed)

Secondary

MeasureTime frameDescription
Bone Density3 months after surgeryCBCT (change is being assessed)

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026