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OpenTrials
Completed

NCT Number: NCT05351463

Papilla Suture Design Affects Papillary Postsurgical Dimensions

The current prospective, randomized, controlled clinical trial aimed at comparing the impact of papillae suture technique on interdental papilla dimensions after periodontal surgery using a novel 3D intraoral scanning technique.

Completed

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hadassah Medical Organization, Jerusalem, Israel

Jerusalem, Israel

About this study

Scientific rationale for study: Choosing the appropriate suture design for periodontal surgery may affect post-surgery tissue dimension. This is a critical issue in periodontal surgery due to the grave impact papilla play on soft tissue esthetics.

Principal findings: using the novel 3D scanning of the gingiva tissue show that simple interrupted suture negatively affect post-surgery papillary height and recession adjacent to the suture compared with vertical internal mattress suture.

Practical implications: the study provide evidence that allows the clinician to better choose the suture design that will allow optimal healing of the papilla. Furthermore, the study presents a novel 3D scanning method to analyzed dimensional changes in the soft tissue.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • 18 years or older
  • Systemically healthy (based on health questionnaire prior to treatment)
  • Willingness to participate in the study
  • Clinical requirement for periodontal\\ implant surgery

Exclusion criteria

  • Diagnosis of diabetes/heart disease, thrombocytopenia\\ coagulation factors deficiency
  • Chronic use\\abuse of drugs\\ alcohol
  • Pregnancy Smoking more than 10 cigarettes per day Antibiotic consumption in the last 3 months.

Treatment and study plan

papila suture technique

Procedure

simple interupted vs internal horoizontal matress suture

Primary outcomes

  1. papilary volume

    Time frame: 12 weeks post surgery

    changes in papilary volume using 3D scanner

Sponsors and collaborators

Lead sponsor

Hadassah Medical Organization

Other

Registry information

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Apr 28, 2022
Registry last updated
Apr 28, 2022

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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