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Comparison of Effectiveness of Gingival Displacement Using Retraction Cord and Aluminum Chloride Gel

D

Dow University of Health Sciences

Status and phase

Enrolling
Phase 4

Conditions

Gingival Bleeding
Tissue Injury
Prosthesis Failure, Dental

Treatments

Device: knitted cotton retraction cord
Device: aluminum chloride gel

Study type

Interventional

Funder types

Other

Identifiers

NCT07255976
Dr Armeen Fakhur

Details and patient eligibility

About

This study aims to compare the horizontal gingival displacement by using a retraction cord and aluminum chloride gel, and also to determine the time taken for placement and hemorrhage after the procedure by using a retraction cord and aluminum chloride gel. Patients of both genders, age ranges from 18 to 50 years, will be selecting requiring fixed prosthesis with of minimum two abutments. This study divided in two parallel groups of 33 patients in each group.

Full description

To compare the effectiveness of a knitted retraction cord and 25% aluminum chloride-containing gel for horizontal gingival displacement, time taken for placement, patient discomfort and bleeding control after retraction cord removal and gel application with improved quality and better marginal fit of fixed prosthesis. This study include patients from range 18 to 50 years, Finishing line margins will be equigingival,Clinically and by radiographic analysis, healthy gingiva and periodontium around the abutments. Bleeding on probing index score-0 included,plaque index score(1-3) not included.

exclusion criteria is Sub-gingival or supra-gingival margins Patient having inappropriate root canal treated tooth. i.e Periapical pathosis over obturation, short root canal,Patient with probing depth 3mmm and above with uncontrolled bleeding. Patient with uncontrolled diabetes, hypertension or neurological disease.

SAMPLE TECHNIQUE: Non- probability consecutive sampling technique. Two groups will be formed among 66 patients with control group is retraction cord group and make two impressions after crown preparation with a finishing line Equiogingival margins will form than in group A in this study apply knitted retraction cord ultra Pak in thickness of .oo mm through retraction cord instrument by cord pecker retraction gel by company provided disposable tips with syringe into the circumferential area of sulcular preparation for 2 minutes and group B using gingival retraction gel containing 25% aluminum chloride viscous tat by ultra-dent after application of gingival retraction gel into sulcular area for 1-3minutes and wash with firm air water spray and will make impressions by one-step technique putty with the light body in metal stock trays then remove and check the impression for any inaccuracy then disinfect the impressions and pores with type 2 hard plaster and mention the code over cast that will not mix. The time required for placement of both gingival retraction systems will be recorded by using stopwatch in seconds and haemorrhage control will be checked by clinically observed with the naked eyes after air water spray up to 3 -5 seconds comparison of horizontal displacement on cast will be analyzed by stereomicroscope images using image analysis software at Dow dental lab.

Enrollment

66 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. age ranges from 18 to 50 years a fixed prosthesis with minimum of two abutments.
  2. minimum of two abutments
  3. Finishing line margins will be Equiogingival
  4. Clinically healthy gingiva and periodontium.

Exclusion criteria

  • 1. Sub-gingival or supra-gingival margins 2 Periapical pathosis 3. inadequate obturated root canals 4. bleeidng disorder 5.uncontrolled diabetes, 6.hypertension 7.neurological disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

66 participants in 2 patient groups

Retraction cord
Active Comparator group
Description:
Conventionally used knitted cotton retraction cord
Treatment:
Device: knitted cotton retraction cord
Aluminum chloride gel
Experimental group
Description:
experimental 25% aluminum chloride gel retraction
Treatment:
Device: aluminum chloride gel

Trial contacts and locations

1

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Central trial contact

Armeen Fakhur, bds

Data sourced from clinicaltrials.gov

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