Health TrialsbyHealthPanel

NIPSA Versus Marginal Approach by Palatal Incision and MIST in Periodontal Regeneration

ConditionsPeriodontitisPeriodontal DiseasesPeriodontal Pocket
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversidad de Murcia

About this trial

Three techniques for periodontal reconstruction will be compared, in which marginal access versus apical access will be carried out.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients diagnosed with periodontitis.

plaque index and bleeding index of < 30%.

periodontal lesions with pocket probing depth > 5 mm.

intrabony defect > 3 mm.

Disqualifiers

patients with systemic diseases that contraindicated treatment.

third molars.

teeth with incorrect endodontic or restorative treatment.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Non-incised papillae surgical approach (NIPSA)

    Procedure/Surgery

    Periodontal reconstructive surgery

  • marginal approach by palatal incision

    Procedure/Surgery

    Periodontal reconstructive surgery

  • Minimally invasive surgical technique (MIST)

    Procedure/Surgery

    Periodontal reconstructive surgery

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: Non-incised papillae surgical approach (NIPSA)Experimental treatment 1 intervention
Group B: marginal approach by palatal incisionActive comparator 1 intervention
Group C: Minimally invasive surgical technique (MIST)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Probing pocket depth (PD)

Probing pocket depth will be assessed with a periodontal probe, measured in mm from the gingival margin to the bottom of the pocket

Time frame
12 months
2

Clinical attachment level (CAL)

Clinical attachment level will be assessed with a periodontal probe, measured in mm from the cementoenamel junction (CEJ) to the bottom of the pocket.

Time frame
12 months
3

Recession (REC)

Recession, will be assessed with a periodontal probe, measured in mmm on the buccal aspect, from the CEJ to the gingival margin zenith.

Time frame
12 months
4

Location of the tip of the papillae (TP)

Location of the tip of the papillae. Taking as reference the level of the mid-axis of the tooth, will be measured the distance from the CEJ at the zenith of the tooth to the tip of the papilla. A positive value will be recorded when the tip of the papillae is located coronally to the CEJ and a negative value otherwise. This outcome will be assessed with a periodontal probe and measured in mmm.

Time frame
12 months

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Universidad de Murcia

Lead sponsor

Source ClinicalTrials.gov
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