Subgingival Clamp Versus Retraction Cord in Cervical Lesions in Term of Technique Sensitivity and Gingival Health

Sponsor
Cairo University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03917108
Collaborator
(none)
22
2
5

Study Details

Study Description

Brief Summary

assessing subgingival clamp in handling and retracting the gingival tissue at the cervical area to see its effect on the gingival health and its technique sensitivity compared to the most commonly used method (retraction cord), as gingival displacement for cervical restorations affects smile and therefore patient satisfaction with the result.

Condition or Disease Intervention/Treatment Phase
  • Device: retraction cord
  • Device: subgingival clamp
N/A

Detailed Description

Gingival displacement for restoring cervical lesions using retraction cord or subgingival clamp with their technique sensitivity affects the smile as they may cause gingival bleeding, laceration or recession and therefore affects patient satisfaction. There are several methods to achieve retraction; retraction cord is the most commonly used method. It controls the soft tissue displacement, gingival bleeding and expose the margins which provide good visualization and access.

They are effective and safe if the gingiva is healthy, also inexpensive retraction method. However, the use of retraction cord has some disadvantages like: it is time consuming, may cause gingival recession after healing and bleeding after removal, its application needs practice and skill as improper handling of the cord can cause traumatic injuries, gingival recession and marginal exposure of the restoration, it may cause postoperative discomfort and pain for the patient and finally leaving the retraction cord for long time or forgetting to remove it from the sulcus can cause permanent damage to the gingival tissue.

Using gingival retracting clamps with rubber dam isolation prevent the gap caused around the teeth due to vertical and horizontal tissue displacement occurred beneath the area of dento-gingival attachment upon the application of the retraction cord. Also, after clamp stabilization in position, it prevents accidental slippage and trauma to surrounding soft tissue during the restorative procedure. They also provide maximum tissue retraction without laceration of gingival tissues. Also, their availability in different sizes and shapes provide a good adaptation to any tooth configuration and any inaccessible area.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
22 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Other
Official Title:
Assessment of Technique Sensitivity and Gingival Health in Management of Cervical Lesions Performed Using Subgingival Clamp Versus Retraction Cord: A Randomized Controlled Clinical Trial
Anticipated Study Start Date :
May 1, 2019
Anticipated Primary Completion Date :
Sep 1, 2019
Anticipated Study Completion Date :
Oct 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: retraction cord

Device: retraction cord
retraction cord ( Ultra dent sizes #0, #00, #000 ) is placed in the gingival sulcus using blunt instrument and using cotton roll isolation.

Other: subgingival clamp

Device: subgingival clamp
subgingival clamp (KSK clamps W8A, #44, #42, #43) or (Brinker clamps B5, B6) is placed to retract the gingiva with rubber dam isolation

Outcome Measures

Primary Outcome Measures

  1. Time of application [Immediately after application]

    Assessed using timer and the measuring unite is seconds

  2. Number of patients need local anesthesia [Immediately after application]

    It will be measured by patient self assessment for the need of local anesthesia through a Yes/No question

  3. Degree of isolation from cervical fluids [Immediately after application]

    Presence of cervical fluids will be assessed visually using magnifying loup with a Yes/No result

  4. Degree of patient satisfaction [Immediately after application]

    Using visual analogue scale (units on scale from 0-10)

Secondary Outcome Measures

  1. Pink esthetics evaluation [4 month]

    Using a pink esthetic score with a grades from 0-2

  2. Amount of gingival bleeding [4 month]

    Assessed using a score for gingival hemorrhage from 0 -2

  3. Presence of gingival laceration [4 month]

    Occurence of gingival laceration assessed visually using magnifying loup with a Yes/No result

  4. Degree of gingival sensitivity [4 month]

    Assessed using visual analogue scale (units on scale from 0-10)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Subject not less than 18 years of age.

  • Males or females.

  • Have at least one carious or non-carious cervical lesion.

  • Cervical lesions should be equi-gingival or subgingival.

  • Can comply to oral hygiene measures or with good oral hygiene.

  • Have sufficient cognitive ability to understand consent procedures.

  • Vital upper or lower teeth with no signs or symptoms of irreversible pulpitis.

  • Clinically healthy gingiva and periodontium.

  • No evidence of attachment loss, bleeding on probing, or plaque accumulation.

Exclusion criteria:
  • Exclusion Criteria:

  • Patients less than 18 years old.

  • Disabilities (mental health conditions, intellectual disability and physical disabilities).

  • Systemic diseases or severe medically compromised. (Cardiovascular disorder, diabetes, -hypertensive, epileptic.

  • Lack of compliance.

  • Gingival hyperplasia, blood disorder.

  • Attachment loss signs of periodontal disease.

  • Patients contra-indicated for rubber dam placement (Asthmatic patient, mouth breather, -- partially erupted tooth, extremely malposed teeth and latex allergy).

  • Periapical pathosis or signs of pulpal posterior or anterior pathology.

  • Non-vital tooth.

  • Endodontically treated tooth.

  • Sever periodontal affection.

  • Tooth indicated for extraction.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Cairo University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nada Hamada Ahmed Shehab Eldin, principal investigator in Cairo university, Cairo University
ClinicalTrials.gov Identifier:
NCT03917108
Other Study ID Numbers:
  • 603
First Posted:
Apr 16, 2019
Last Update Posted:
Apr 16, 2019
Last Verified:
Apr 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 16, 2019