Dimensional Changes: Randomized Clinical Trial

NCT05684068 | Not Yet Recruiting DMC

• 1 other identifier: 202207368
• Study Type: interventional
• Target: 50
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this clinical trial is to evaluate the dimensional changes in the short and long-term in patients with thin gum tissues who have gum grafts placed on either denuded bone or gum grafts placed on a bone with some tissues remaining. The main question this study aims to answer is: \- Does the placement of free-epithelized gingival grafts (gum grafts) on full thickness bed preparation (having all of the tissue removed from the bone) lead to similar clinical, digital, and patient-related outcomes and measurements over a period of 12 months versus split thickness bed preparation (where a small layer of tissue is left over the bone) in patients with thin gum tissue phenotypes (gum tissue is generally less than 1.5 millimeters) who are in need of soft tissue augmentation procedures? Participants will be asked to attend 8 visits, which include: (i) screening visit, (ii) prophylaxis visit, (iii) random assignment to Group A or Group B along with surgery and digital data collection, (iv) 2-week post-operative visit, (v) 6-week post-operative visit, (vi) 3-month follow-up visit, (vii) 6-month follow-up visit, (viii) 12-month follow-up visit. Also, Group A will have a free epithelialized gingival/mucosal graft (gum graft) placed on full thickness periosteal bed preparation where all of the tissue was removed (test group). Group B will have a free epithelialized gingival/mucosal graft (gum graft) on split thickness periosteal bed preparation where only a portion of the tissue was removed (control group). Researchers will compare Group A and Group B to see if there is a difference in clinical, digital, and patient-related outcomes and measurements over a period of 12 months.

Conditions

Gingival Recession

Outcome Measures

Primary Outcomes (1)

• Change from Baseline in Gingival Thickness as assessed by measurement.

  Tissue changes will be assessed in millimeters and percentage.

  Multiple time points (i.e., Baseline, 3 months, 6 months, 12 months)

Study Arms (2)

Gum Graft Placed on Denuded Bone

EXPERIMENTAL

Subjects in this arm will have a free epithelialized gingival/mucosal graft (gum graft) placed on full thickness periosteal bed preparation where all of the tissue was removed (test group).

Procedure: Gum Graft Placed on Denuded Bone

Gum Graft Placed on Split Thickness Periosteal Bed Preparation

ACTIVE COMPARATOR

Group B will have a free epithelialized gingival/mucosal graft (gum graft) on split thickness periosteal bed preparation where only a portion of the tissue was removed (control group).

Procedure: Gum Graft Placed on Split Thickness Periosteal Bed Preparation

Interventions

Gum Graft Placed on Denuded Bone PROCEDURE

The provider will administer local anesthesia into the subject's gum in order to numb both the subject's donor and recipient areas for gum grafts. Next, the provider will use a surgical blade to dissect the gum graft from the subject's donor site. At the subject's recipient gum recession defect site, the provider will remove all of the subject's tissue, so that the bone is fully exposed before placing a gum graft from the donor site. Afterward, the provider will place sutures in the subject's recipient site in order to promote healing/re-growth.

Gum Graft Placed on Denuded Bone

Gum Graft Placed on Split Thickness Periosteal Bed Preparation PROCEDURE

The provider will administer local anesthesia into the subject's gum in order to numb both the subject's donor and recipient areas for gum grafts. Next, the provider will use a surgical blade to dissect the gum graft from the subject's donor site. At the subject's recipient gum recession defect site, the provider will dissect some of the tissue at the subject's recipient site but still keep a small layer of tissue at the subject's recipient site before placing a gum graft from the donor site. Afterward, the provider will place sutures in the subject's recipient site in order to promote healing/re-growth.

Gum Graft Placed on Split Thickness Periosteal Bed Preparation

Eligibility Criteria

• Age: 18 Years - 95 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients 18-95 years of age
• Inactive periodontal disease
• Lack of, or an insufficient (less than 2 millimeters) band of keratinized tissue width on the buccal site (closest to the cheek)
• Shallow vestibule depth (the space between the soft tissue (lips and cheeks), and the teeth and gums)
• Thin gingival phenotype (less than 1.5mm of gum tissue depth).
• Aberrant frenum attachment in need of free-epithelized gingival grafts.
• At least one RT1, 2, or 3 (Cairo's classification) gingival recession defect on the mandibular anterior sextant (Teeth #22-27).
• Non-smokers or past smokers (those who have stopped at minimum 6 months ago).
• Patient willing and able to follow instruction related to the study procedures.

You may not qualify if:

• Previous soft tissue augmentation procedures at the area of interest.
• Current smokers (Light smokers meaning less than 10 cigarettes/day, heavy smokers meaning more than 10 cigarettes/day, or social smokers)
• Uncontrolled systemic disease (uncontrolled diabetes defined by blood sugar HbA1c greater than 7%)
• Any active local or systemic infections
• Any diseases or medications that may compromise normal wound healing
• Currently receiving chemotherapy or radiotherapy or a history of radiotherapy in head and neck area.
• Severe hematologic (blood) disorders
• Pregnancy or nursing mother
• Patients undergoing orthodontic therapy
• Patients taking antibiotics in the past 3 months

Sponsors & Collaborators

• University of Iowa: lead

Study Sites (1)

University of Iowa College of Dentistry and Dental Clinics

Iowa City, Iowa, 52242, United States

Location

MeSH Terms

Conditions

Gingival Recession

Condition Hierarchy (Ancestors)

Gingival Diseases; Periodontal Diseases; Mouth Diseases; Stomatognathic Diseases; Periodontal Atrophy

Study Officials

• Carlos Garaicoa, DDS, MS

  University of Iowa College of Dentistry

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Carlos Garaicoa Pazmino, DDS, MS

CONTACT

(319) 467-4315; carlos-garaicoapazmino@uiowa.edu

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Clinical Assistant Professor

Study Record Dates

• First Submitted: January 4, 2023
• First Posted: January 13, 2023
• Study Start (Estimated): August 1, 2028
• Primary Completion (Estimated): July 1, 2030
• Study Completion (Estimated): March 1, 2031
• Last Updated: August 19, 2025

Record last verified: 2025-08

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)