The Clinical Usage of a Free Gingival Graft Combined With Frenotomy in Patients With High Frenal Attachment
Status and phase
Conditions
Treatments
Details and patient eligibility
About
In patients with high frenal attachment will placement of free gingival graft combined with frenotomy result in gain of width of keratinized gingiva, decrease relapse, improve mucosal healing and have acceptable postoperative pain?
Full description
In patients with high frenal attachment will placement of free gingival graft combined with frenotomy result in gain of width of keratinized gingiva, decrease relapse, improve mucosal healing and have acceptable postoperative pain?
To the best of our knowledge there aren't any studies discussing the use of free gingival graft in combination with frenotomy procedure to decrease relapse & morbidity of the condition; thus the objective of this case series study is to evaluate the effectiveness of using free gingival graft in combination with frenotomy procedure on increasing the width of keratinized tissue & decreasing relapse, postoperative pain and scar formation.
Inclusion criteria:
Ages 18-40 years old Systemically healthy Gingival and plaque index <10 Good oral hygiene Highly attached mandibular labial frenum. Narrow sulcus depth Thin gingival phenotype
Exclusion criteria:
Smokers Poor oral hygiene Patient with a physical disability that hinders the upkeep of good oral hygiene measures.
Taking any medications that could affect healing Any systemic diseases that delay wound healing. Deep sulcus Thick gingival phenotype Pervious frenal procedures Pregnant or lactating females Pervious periodontal surgery within the last 6 months before the start of the trial
Interventions
Preoperative measures:
- All subjects will pass through phase I therapy (Supragingival scaling, subgingival debridement and oral hygiene instructions) before any surgical procedures.
- After 4 weeks, all subjects will be examined to determine patient compliance with oral hygiene procedures (tooth brushing twice daily and chlorhexidine HCL 1.25% mouthwash twice daily).
- Eligible & complied patients will be enrolled in the study
Intervention - Surgical Phase (T0):
- The same operator (M S) will perform all procedures.
- After following complete aseptic precautions, surgical technique will be performed. Local infiltration will be done using local anaesthetic solution 4% articaine with 1/200 000 adrenaline solution.
- A horizontal incision will be placed at mucogingival junction using 15c blade with respect to teeth 42,41,31,32, which is then followed by supraperiosteal dissection or frenal relocation of the mandibular labial frenum up to the desired level using periosteal elevator.
- Undermining the edges of the frenum using periosteal elevator separating the epithelium from the underlining lip mucosa.
- The mucosa is sutured in the periosteum by using simple interrupted suture at the desired new level of the frenum.
- Gauze moistened with saline is to be placed over the recipient bed until graft placement.
- A free gingival autograft will be harvested from the palate using 15c blade and tissue forceps.
- Stabilization of the free gingival autograft in place using a 6-0 resorbable Vicryl suture using combination of interrupted and sling sutures.
Post-operative care:
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Patients abstained from tooth brushing for 2 days post-operatively.
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Using 0.2% cholohexidine mouthwash twice daily for 14 days to be started on the 2nd day of surgery.
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Ibuprofen 600 mg 1 tablet PRN.
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Patients will be instructed to:
- Follow the instructions completely.
- Keep up a strict follow-up schedule.
- Brush their teeth twice a day, with a soft brush, and avoid brushing the surgical area (to be started 2 days post-surgery).
- Not to touch the surgical area, with the tongue or fingers.
- Do not wear any kind of dental appliances, on or around the surgical site.
- Not to eat or bite on the anterior teeth during the healing period.
Follow-up (T1, T2,T3, T4):
T1 1. Patients recalled after 5 days for measurement of mucosal healing using IPR (Inflammatory, Proliferativ, & Remodeling) Wound Healing Scale (Hamzani & Chaushu, 2018).
T2
- Patients recalled after 14 days for suture removal.
- Measurement of pain score using Numerical Rating scale (NRS) measurement. (Williamson & Hoggart, 2005).
- Measurement of mucosal healing using IPR (Inflammatory, Proliferativ, & Remodeling) Wound Healing Scale (Hamzani & Chaushu, 2018).
T3
- Patients recalled after 2 months.
- Measurement of mucosal healing using IPR (Inflammatory, Proliferativ, & Remodeling) Wound Healing Scale (Hamzani & Chaushu, 2018).
T4
- Patients recalled after 3 months for the evaluation of frenum relapse using periodontal probe (Sarmadi et al., 2021).
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Ages 18-40 years old
- Systemically healthy
- Gingival and plaque index <10
- Good oral hygiene
- Highly attached mandibular labial frenum.
- Narrow sulcus depth
- Thin gingival phenotype
Exclusion criteria
- Smokers
- Poor oral hygiene
- Patient with a physical disability that hinders the upkeep of good oral hygiene measures.
- Taking any medications that could affect healing
- Any systemic diseases that delay wound healing.
- Deep sulcus
- Thick gingival phenotype
- Pervious frenal procedures
- Pregnant or lactating females
- Pervious periodontal surgery within the last 6 months before the start of the trial
Trial design
Primary purpose
Allocation
Interventional model
Masking
12 participants in 1 patient group
Trial contacts and locations
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Central trial contact
Manal Hosny, Professor; Mohammed S. Saleh, Bachelor
Data sourced from clinicaltrials.gov
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