Role of GTR on Healing Outcome & Quality of Life in Combined Endo Perio Lesions With Communication

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age16+
SponsorPostgraduate Institute of Dental Sciences Rohtak

About this trial

The recovery of periapical defects linked to periodontal communication frequently yields less satisfactory results. Numerous studies and case reports have highlighted the notable success achieved through the application of guided tissue regeneration techniques. More recently, autologous platelet concentrate plug \& placental membrane have emerged as a treatment option for addressing such lesions. Nevertheless, there has been no study using PRF-Medium with ACM membrane on the healing of aforesaid lesion \& quality of life assessment.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients of age 16yrs and above.

Patients with apico-marginal defects and deep pocket upto apex of tooth.

Failed primary root canal treatment.

Presence of interproximal bone loss.

Disqualifiers

Presence of vertical root fracture

Presence of root perforations

ASA-3 or ASA-4 according to the classification of the American Society of Anesthesiologists)

Presence of root resorption

Trial design

Design model

Parallel

Treatments tested in this trial

  • Endodontic Micro-Surgery

    Procedure/Surgery

    Surgery performed using ACM membrane and PRF plug in test group \& without membrane \& PRF in control group.

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Pt with apicomarginal defects & interproximal bone loss receiving GTRExperimental treatment 1 intervention
Group B: Pt with apicomarginal defects & interproximal bone loss without GTRActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Periapical healing assessment

Periapical healing comparison in 2 groups 2D radiographic healing by Rud et al and Molven et al criteria and 3D healing by modified PENN 3D Criteria. Healing will be categorised into complete, incomplete, uncertain, unsaisfactory.

Time frame
Base line to 12 months

Secondary outcomes

1

Quality of life assessment

to assess pain, swelling, mouth opening and effect on daily activities of patient among test and control group using OHIP-14 questionnaire. Pain Assesment with Value 0 indicate no pain \& 100 indicate maximum pain.

Time frame
Base line to 12 months

Other outcomes

Sponsors and contacts

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