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NCT Number: NCT06588998

Xengenic Cortical Membranes Versus Connective Tissue Graft With Coronally Advanced Flap for the Treatment of Peri-implant Soft Tissue Dehiscences: A Randomized, Controlled Clinical Trial

Peri-implant soft tissue dehiscences represent a common complication in implant dentistry, often leading to esthetic and functional challenges. Current treatment options, including Xengenic cortical membranes and connective tissue graft with coronally advanced flap, aim to promote soft tissue regeneration and improve clinical outcomes. However, there is a need for comparative studies to determine the optimal treatment modality for peri-implant soft tissue dehiscences.

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Key information

Conditions

Immediate Implant Connective Tissue Graft

Age range

20 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

TantaU

Tanta, Gharbia Governorate, Egypt

Location status: Recruiting

About this study

Aim: Comparing the effectiveness and patient outcomes of Xengenic cortical membranes versus connective tissue graft with coronally advanced flap for the treatment of peri-implant soft tissue dehiscences.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults (20-50) years old. •peri-implant soft tissue dehiscence . •Thin gingival phenotype. •Optimal compliance as evidenced by no missing treatment appointments and positive attitude towards oral hygiene.

Exclusion criteria

  • •Medically compromised patients and systemic conditions precluding implant and periodontal surgery. •Smokers, diabetics, pregnant or lactating women. •History of chemotherapy, radiotherapy in head and/or neck region. •Bisphosphonate therapy.

Treatment and study plan

Xengenic Cortical membranes

Device

soft tissue surgery around dental implant dehiscence

Other names: Osteobiol ,flexible xenograft cortical sheet from Technoss,USA

connective tissue graft

Procedure

soft tissue surgery around dental implant dehiscence

Primary outcomes

  1. peri implant soft tissue thickness

    Time frame: six months

Secondary outcomes

  1. pink esthetic score

    Time frame: six months

Study contacts

Contact information is provided by the study sponsor or research team.

amr anwar ellithy, MSC

CONTACT

[email protected]

00201066767062

bassem nabil elfahl, PHD

CONTACT

+20 114 009 0390

Sponsors and collaborators

Lead sponsor

Amr Anwar Mohamed Ellithy Yousef

Other

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Sep 19, 2024
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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