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Evaluation of Healing of Intra-bony Defects in Modified Minimal Invasive Surgical Technique

Clinical and Radiographic Evaluation of Intra Bony Defects Following Complete Versus Incomplete Removal of Granulation Tissue in Modified Minimally Invasive Surgical Technique (M-MIST). A Randomized Controlled Clinical Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03562039
Enrollment
16
Registered
2018-06-19
Start date
2018-04-15
Completion date
2021-04-03
Last updated
2024-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Periodontal Regeneration, Clinical and Radiographic Results, Modified Minimal Invasive Surgery

Brief summary

This study is aiming to compare the clinical and radiographic outcomes after complete versus incomplete removal of granulation tissue during modified minimally invasive surgical technique for management of periodontal intrabony defects in patients with chronic periodontitis.

Detailed description

Periodontal surgery has been expanding in the world of dentistry throughout the past years, as new techniques are emerging to treat the different and complex periodontal disorders. Surgical procedures in dentistry have undergone major changes to minimize invasiveness. In addition, novel instruments and materials have been made to suit the evolution of the surgical procedures (Cortellini. 2012). Teeth with deep pockets associated with deep intra-bony defects are a clinical challenge for periodontists, where periodontal regeneration has been proven to be effective in managing the treatment of one-, two-, and three-wall intra-bony defects (Needleman and Tucker 2012;Needleman. 2015). Harrel and Rees (1995) were the first to introduce the term minimally invasive surgery (MIS). MIS is used to describe the use of smaller and more precise surgical procedures that are possible by using of magnifying instruments, such as operating microscopes and microsurgical instruments and materials (Cortellini. 2012). The rationale for the development of minimally invasive surgical technique (MIST) includes: reduction of trauma during the surgery, increase in flap and wound stability, improvement of wound primary closure, reduction of surgical time, and minimization of intra-operative and post-operative patient discomfort (Cortellini. 2007). With the use of MIST, Cortellini and Tonneti (2009) confirmed blood clot protection with the aspects of wound and blood clot stability and primary wound closure. An enhancement of MIST, the modified minimally invasive surgical technique (M-MIST), has been introduced by Cortellini in 2009 to further reduce the surgical invasiveness, with three major objectives in mind: (1) minimize the interdental tissue tendency to collapse providing space provision for regeneration, (2) enhance the wound/soft tissue stability and (3) reduce patient morbidity. Some authors evaluated the use of various regenerative material in MIST and M-MIST e.g. Enamel matrix derivative (Cortellini 2007) PDGF-bb (Cosyn et al. 2012) and collagen enriched bovine derived xeno-graft (Mishra et al., 2013). Cortellini (2011) also, noted that the use of regenerative material is not necessary with M-MIST. Hung et al, (2012) reported that granulation tissue could contain progenitor stem cells which are very important components needed for periodontal tissue regeneration. Moreover, Park et al. (2011) assumed that the inflamed granulation tissue could be used to regenerate lost tissues in the same individual in other defective sites according to its regenerative potential. All the previous data raised an important question about the necessity to remove granulation tissues in periodontal regenerative techniques: Is complete removal of granulation tissue in M-MIST is mandate for treating isolated intra-bony defects for better healing?

Interventions

PROCEDUREM-MIST

minimal invasive surgical technique without thorough removal of granulation tissue

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* \- systemically healthy patients * Age range from 25 - 55. * Patients with moderate to advanced chronic periodontitis with pockets ≥ 5 mm 6-8 weeks after phase I (non-surgical) therapy. * Vertical 2 or 3 walls Intra-bony defects. * Perform and maintain good oral hygiene. * Able to come for the follow up appointment's needed

Exclusion criteria

* \- Smokers. * Pregnant patients. * patients with poor oral hygiene. * Multirooted teeth with furcation involvement.

Design outcomes

Primary

MeasureTime frameDescription
changes in clinical attachment levelat baseline then 6, 9 and 12 monthsIt is the distance from the cement-enamel junction to the depth of the pocket.

Secondary

MeasureTime frameDescription
changes in pocket probing depthat baseline then at 6, 9 and 12 monthsdistance from the depth of the pocket to the gingival margin
changes in gingival recessionat baseline then at 6, 9 and 12 monthsdistance of the exposed root surface from the cemento-enamel junction to the gingival margin
amount of bone fillat baseline then at 6, 9 and 12 monthsdifference in bone fill in standardized periapical radiograogh
patient pain and discomfortat day of the surgery then at 1 , 3 and 7 days post-surgeryby giving the patient a questionnaire to fill
patient satisfaction12 months post-surgeryby giving the patient a questionnaire to fill

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026