← Back to Clinical Trials
Recruiting NCT06030947

NCT06030947 Effectiveness of Micro Connective Tissue Graft for Treatment of Multiple Adjacent Gingival Recession Defects

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06030947
Status Recruiting
Phase
Sponsor Göteborg University
Condition Gingival Recession, Localized
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2025-03-01
Primary Completion 2026-01-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 60 Years
Study Type INTERVENTIONAL
Interventions
Coronally Advanced Flap combined with a Connective Tissue GraftCoronally Advanced Flap combined with micro Connective Tissue GraftDivision of the Connective Tissue Graft into multiple micro Connective Tissue Grafts

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 30 participants in total. It began in 2025-03-01 with a primary completion date of 2026-01-01.

⚠ 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

The objective of this project is to evaluate 1-year outcomes of treatment of MAGRD using a modified coronally advanced tunnel technique (MCAT) with either conventional CTG (control group) or micro-CTG (test group).

Eligibility Criteria

Inclusion Criteria: * age ≥18 years, * systemically healthy, * presenting with a minimum of 4 and a maximum of 6 adjacent RT1/RT2 recessions, located in the maxilla or mandible with an apico-coronal extension (i.e. recession depth) of ≥2 mm, * Full-Mouth Plaque Score (FMPS) \<20%, * Full-Mouth Bleeding Score (FMBS) \<20%. Exclusion Criteria: * pregnancy or lactation, * tobacco smoking, * uncontrolled medical condition, * medication that can affect gingival conditions. * thick phenotype, * severe tooth malpositioning, * uncorrected trauma from toothbrushing, * a previous history of root coverage procedures * the presence of furcation defects.

Contact & Investigator

Central Contact

Olivier Carcuac, DDS, PhD

✉ olivier.carcuac@gu.se

📞 556275575

Principal Investigator

Jan Derks, DDS, PhD

STUDY CHAIR

Goteborg University

Frequently Asked Questions

Who can join the NCT06030947 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 60 Years, studying Gingival Recession, Localized. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06030947 currently recruiting?

Yes, NCT06030947 is actively recruiting participants. Contact the research team at olivier.carcuac@gu.se for enrollment information.

Where is the NCT06030947 trial being conducted?

This trial is being conducted at Dubai, United Arab Emirates.

Who is sponsoring the NCT06030947 clinical trial?

NCT06030947 is sponsored by Göteborg University. The principal investigator is Jan Derks, DDS, PhD at Goteborg University. The trial plans to enroll 30 participants.

Related Trials

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: September 2026  ·  Data Methodology