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Effect of Different Suturing Technique on Height of Interdental Papilla and Periodontal Healing

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ClinicalTrials.gov Identifier: NCT03429764
Recruitment Status : Recruiting
First Posted : February 12, 2018
Last Update Posted : February 12, 2018
Sponsor:
Information provided by (Responsible Party):
Postgraduate Institute of Dental Sciences Rohtak

Brief Summary:

Comparative clinical evaluation of internal mattress sutures vs continuous independent sling sutures on interdental papilla height and periodontal healing in esthetic zone.

To evaluate the effect of internal mattress suturing technique on interdental papilla height and periodontal healing after periodontal surgery in esthetic zone.

To evaluate the effect of continuous independent sling suturing technique on interdental papilla height and periodontal healing after periodontal surgery in esthetic zone.


Condition or disease Intervention/treatment Phase
Gingival Papillary Blunting Procedure: CISS Procedure: VIMS Not Applicable

  Show Detailed Description

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 36 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Comparative Clinical Evaluation of Internal Mattress Sutures vs Continuous Independent Sling Sutures on Interdental Papilla Height and Periodontal Healing in Esthetic Zone: Randomized Clinical Study
Actual Study Start Date : December 1, 2017
Estimated Primary Completion Date : February 2019
Estimated Study Completion Date : February 2019

Arm Intervention/treatment
Active Comparator: Control group (CG),CISS
continuous independent sling sutures (CISS) will be placed with minimum two intact contact points at the surgical site,
Procedure: CISS
continuous independent sling sutures will be placed with minimum two intact contact points at the surgical site

Experimental: Test group (TG),VIMS
internal mattress suture (VIMS) will be placed with minimum two intact contact points at the surgical site,
Procedure: VIMS
internal mattress suture will be placed with minimum two intact contact points at the surgical site




Primary Outcome Measures :
  1. inerdental papilla height [ Time Frame: 6 months ]
    effect on interdental papilla height,

  2. CAL [ Time Frame: 6 months ]
    Gain in clinical attachment level



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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Patient with age 18-65 years and who are systemically healthy.
  2. Possessing ≥20 natural teeth
  3. Patient with chronic periodontitis ( armitage classification)36
  4. Pocket depth ≥ 5mm in maxillary esthetic zone
  5. Completed etiological periodontal therapy (oral hygiene instructions and scaling and root planning with full-mouth bleeding score FMBS <20% and plaque index score<1 (sillness n loe)37

Exclusion Criteria:

  1. Smokers (current and past) and tobacco chewers.
  2. Medically compromised patients.
  3. Patient on long term use of drugs which could affect the treatment and final outcome of the surgery.
  4. Patient under systemic antibiotics in past 6 month.
  5. Pregnant women and lactating mothers.
  6. Patient who had undergone periodontal treatment 6 months prior to the study.
  7. Patients who are allergic to materials or drugs used in study.
  8. Patients having loss of contact point in adjacent teeth

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03429764


Contacts
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Contact: Nishi Tanwar, MDS 8368126310 nsh_tanwar@yahoo.co.in

Locations
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India
Post Graduate Institute of Dental Sciences Recruiting
Rohtak, Haryana, India, 124001
Contact: NISHI TANWAR, MDS    8368126310    nsh_tanwar@yahoo.co.in   
Sponsors and Collaborators
Postgraduate Institute of Dental Sciences Rohtak
Investigators
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Principal Investigator: RASHMI SUHAG Post graduate institute of dental science Rohtak

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Responsible Party: Postgraduate Institute of Dental Sciences Rohtak
ClinicalTrials.gov Identifier: NCT03429764     History of Changes
Other Study ID Numbers: Rashmiperio
First Posted: February 12, 2018    Key Record Dates
Last Update Posted: February 12, 2018
Last Verified: January 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No