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Papilla Suture Design Affects Papillary Postsurgical Dimensions

H

Hadassah Medical Center

Status

Completed

Conditions

Oral Surgery
Periodontal Surgery

Treatments

Procedure: papila suture technique

Study type

Interventional

Funder types

Other

Identifiers

NCT05351463
HMO-0079-15

Details and patient eligibility

About

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.

Full description

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.

Enrollment

20 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

one arm study
Other group
Description:
in each case one site was assigned as control site and one site was assigned as test site.
Treatment:
Procedure: papila suture technique

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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