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Recruiting NCT07532694

NCT07532694 Diode Laser-Assisted Periodontal Therapy in Kidney Transplant Recipients

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Clinical Trial Summary
NCT ID NCT07532694
Status Recruiting
Phase —
Sponsor Military Hospital 103
Condition Periodontitis
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2025-12-09
Primary Completion 2026-06-09

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Scaling and Root PlaningDiode Laser

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 80 participants in total. It began in 2025-12-09 with a primary completion date of 2026-06-09.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This randomized controlled trial evaluates the efficacy of diode laser-assisted non-surgical periodontal therapy in kidney transplant recipients with periodontitis. Eighty participants will be allocated to two parallel groups: scaling and root planing (SRP) with adjunctive diode laser therapy or SRP alone. Clinical periodontal parameters, blood biomarkers, radiographic findings, and subgingival microbiome profiles will be assessed at baseline and during follow-up. The study aims to determine whether adjunctive diode laser therapy provides superior clinical and biological improvement compared with SRP alone.

Eligibility Criteria

Inclusion Criteria: * Kidney transplant recipients aged 18 years or older. * Diagnosis of periodontitis according to the study case definition. * Medically stable and able to undergo non-surgical periodontal treatment. * Willing and able to provide written informed consent and attend follow-up visits. Exclusion Criteria: * \- Periodontal treatment or systemic antibiotic use within the predefined exclusion window in the protocol. * Acute oral infection requiring urgent treatment. * Pregnancy or lactation, if excluded by the approved protocol. * Serious systemic condition or clinical instability judged by investigators to preclude study participation. * Inability to comply with study procedures or follow-up schedule.

Contact & Investigator

Central Contact

Thang V Dinh, Principal Investigator

✉ bsdinhthang277@gmail.com

📞 +84971349066

Frequently Asked Questions

Who can join the NCT07532694 clinical trial?

This trial is open to participants of all sexes, studying Periodontitis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07532694 currently recruiting?

Yes, NCT07532694 is actively recruiting participants. Contact the research team at bsdinhthang277@gmail.com for enrollment information.

Where is the NCT07532694 trial being conducted?

This trial is being conducted at Hanoi, Vietnam, Hanoi, Vietnam.

Who is sponsoring the NCT07532694 clinical trial?

NCT07532694 is sponsored by Military Hospital 103. The trial plans to enroll 80 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology