Clinical Trial Details
— Status: Not yet recruiting
Administrative data
NCT number |
NCT05579522 |
Other study ID # |
PER313 |
Secondary ID |
|
Status |
Not yet recruiting |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
October 10, 2022 |
Est. completion date |
April 1, 2024 |
Study information
Verified date |
October 2022 |
Source |
Cairo University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
The goal of this randomized controlled trial is to evaluate the amount of interdental papilla
fill following the injection of the fat graft compared to hyaluronic acid filler in patients
with interdental papilla deficiency. Highly motivated patients having at least one deficient
papilla with the presence of a contact point between adjacent teeth in the inter-bicuspid
region. Papillary deficiency types I or II, according to Nordland and Tarnow
(1998)classification will be selected. The main question it aims to answer is: In patient
with interdental papillary deficiency, will injecting autogenous fat increase papilla height
compared to hyaluronic acid injection? Participants in the test group will receive fat graft
injection in the inter dental papilla. In the injection phase, 3 injections will be given at
each papilla site: at baseline, 3 and 6 weeks intervals. While in the control group,
hyaluronic acid injection in the interdental papilla and also 3 injections will be given at
each papilla site at the same intervals.
Description:
The treatment protocol will be divided into 3 phases: the pre-operative phase, where patients
will be examined for eligibility, the treatment phase, where both control and interventional
treatments will be carried out and finally the follow up phase, where patients will be
followed up for the duration of the study.
A- Preoperative Evaluation A.1. Medical History A thorough detailed personal and dental
history will be collected from all patients. Medical evaluation will be done before enrolling
patients in the study to exclude the presence of any disease that may contraindicate
treatment or exclude the patient from the study.
A.2. Clinical evaluation Initial periodontal therapy including full mouth supragingival
scaling and subgingival debridement and patient motivation and education for proper oral
hygiene.
After 6 weeks, re-evaluation of the deficient papilla will be done, and the degree of
papillary deficiency according to Nordland and Tarnow classification [13] will be determined.
Plaque and gingival indices will also be assessed and used to determine eligibility. Only
patients with deficient papilla fulfilling the inclusion criteria will be recalled discussing
all treatment options and sign the informed consent.
Once enrolled in the study, alginate impression will be taken for the involved arch/arches to
construct study casts and fabricate customized stents to standardize measurements throughout
the study. Standardized digital clinical photographs will also be taken for the GBT as a
baseline measurement of the dimension of the black triangle. One-week later patients will be
scheduled for the 1st injection.
A.3. Radiographic evaluation The distance between the contact area and inter-proximal bone
crest (CP-BC) will then be measured to determine eligibility at the sites of papillary
deficiency using peri-apical radiographs with paralleling technique and then confirmed by
bone sounding.
B- Treatment phase:
In the injection phase, 3 injections will be given at each papilla site: at baseline, 3 and 6
weeks intervals.
1. Clinical measurement of the height of the black triangle will be by measuring the
distance between the deficient papilla tip and contact area (PT-CP distance) to the
nearest 0.5 mm (baseline). This will be done using a graduated periodontal probe and the
fabricated customized stent for proper and standardized positioning of the probe at each
measurement interval.
2. Standardized digital clinical photographs will be taken for the eligible deficient
papillae for the baseline measurement of the surface area of black triangles.
3. Local anesthesia will be administered by infiltration to achieve the necessary
anesthesia to allow a comfortable treatment procedure.
4. Patient allocation concealment will be broken to determine will treatment:
The patient will be randomly assigned to one of the treatment groups:
- Group A (Test): Fat graft injection in the inter dental papilla.
- Group B (Control): Hyaluronic acid injection in the interdental papilla.
Control group (Hyaluronic acid injection in the interdental papilla):
- The deficient papilla will be injected with 0.1 mm of HA gel concentration of 20 mg/ml
using a 30-gauge disposable insulin syringe.
- The needle will be inserted 2-3 mm apical to the tip of the interdental papilla and
directed coronally with an angulation of 45° to the long axis of the tooth, and the
bevel directed apically.
- The papilla will be lightly molded in an incisal direction for 1 minute using gauze.
Test group (Fat graft injection in the inter dental papilla):
- Free buccal fat graft will be harvested from the buccal pad of fat.
- After administering anesthesia in the posterior area at the depth of the vestibule, a
small horizontal incision in the free mucosa above the second and the third maxillary
molars will be created using a sharp #11 blade.
- Through blunt dissection, the fat tissue will be accessed and easily mobilized into the
oral cavity by progressive blunt dissection.
- The desired amount of fat will be harvested, and the remaining buccal pad will be pushed
back in its place.
- Interrupted sutures with 5-0 vicryl resorbable sutures will be used to achieve primary
closure of the incision.
- The fat graft will be rinsed to remove any debris and mechanically emulsified.
Fat emulsification
- Emulsification of the fat will be done by shifting the fat between two 10-cc syringes
connected to each other by a female-to-female Luer-Lok connector processing the block
fat graft into nano-fat (Tonnard et al., 2013).
- After 30 passes, the fatty liquid will be filtered over a sterile nylon cloth and the
fluid will be collected in a sterile syringe. This is done to remove any connective
tissue remnants that could block the fine needles.
- A 30-gauge disposable insulin syringe will be used to load the nano-fat graft and will
be inserted 2-3 mm apical to the tip of the interdental papilla.
Postoperative phase:
After completion of the treatment, self-care instruction will be given to the patients
Patient self-care instructions (Heitz-Mayfield 2008):
- Avoid mechanical plaque control in the area for 24 hours after the injection.
- Oral hygiene should be maintain using a soft toothbrush after the first 24 hours.
- Antiseptic mouth rinse, Chlorhexidine mouth rinse will be prescribed twice per day for
two weeks.
Follow up and post-operative evaluation Patients will be recalled after 3 and 6 months from
the first injection where clinical measurement of the gingival black triangle dimensions and
standardized digital clinical photographs will be retaken.
The outcomes are:
1. Black triangle height
- The black triangle height (BTH) will be assessed using standardized digital
clinical photographs and analyzed by an image analysis program (Photoshop Cs 5,
Adobe Systems, San Jose, CA, USA).
- Method of aggregation: Mean
- Specific measurement time point: at baseline, after 3 weeks, 6 weeks and 6 months
postoperatively.
2. Black triangle area
- The surface area of the black triangle (BTA) will be assessed using standardized
digital clinical photographs and analyzed by an image analysis program (Photoshop
Cs 5, Adobe Systems, San Jose, CA, USA).
- Method of aggregation: Mean
- Specific measurement time point: at baseline, after 3 weeks, 6 weeks and 6 months
postoperatively.
3. Black triangle width
- The black triangle width (BTW) will be assessed using standardized digital clinical
photographs and analyzed by an image analysis program (Photoshop Cs 5, Adobe
Systems, San Jose, CA, USA).
- Method of aggregation: Mean
- Specific measurement time point: at baseline, after 3 weeks, 6 weeks and 6 months
postoperatively.
4. Post-Surgical Patient Satisfaction:
- A 3-item questionnaire will be asked to the patients and a VAS scale for 0-10 will
be used.
- These items will be: Would you experience the same procedure another time? To what
extent are you satisfied about the procedure? To what extent are you satisfied with
the results?
5. Post-operative pain Visual Analogue Scale (VAS) with numbers from 0 to 10 ('no pain' to
'worst pain imaginable') will be measured at 24 hours.
Criteria for Discontinuing or Modifying Intervention:
Intervention will be discontinued or modified if the patient is unable to commit to the
follow-up schedule or has any conditions that prevents him/her to continue the study.
Strategies to improve adherence to intervention:
- Patients will be recalled monthly for supportive periodontal therapy during the course
of the study.
- Close follow up by phone will be done to ensure patient engagement