Evaluation of Different Gingival Retraction Systems on Gingival Displacement and Periodontal Health (retraction)
Gingival Hemorrhage
About this trial
This is an interventional treatment trial for Gingival Hemorrhage
Eligibility Criteria
Inclusion Criteria:
- forty patients whose ages more than 18 years were selected requiring fixed prosthesis with minimum of two abutments.
- Clinically and radiographically healthy gingiva and periodontium around the abutments.
- Abutment teeth of normal size and contour (no developmental anomaly or regressive age changes).
Exclusion Criteria:
- Age <18 years.
- Gingival and periodontal disease.
- Uncontrolled diabetes, hypertension, hyperthyroidism and other cardiovascular disorders.
Sites / Locations
- Cairo UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Active Comparator
Active Comparator
Experimental
Placebo Comparator
Gingitrac
traxodent
Ultrapk cord
nocord
The gingitrac cartridge was attached to the automixing gun and then the mixing syringe with intraoral tip was placed into the gingival sulcus and gingival retraction material was applied all around the selected abutment. After injecting the retraction material ,the corresponding comprecap was placed on to the abutment to push the material deep into the gingival sulcus. After 4 min, the comprecap with the set retraction material attached to it was removed from the patient mouth.
The traxodent cartridge was attached to the automixing gun and then the mixing syringe with intraoral tip was placed into the gingival sulcus and gingival retraction material was applied all around the tooth. After injecting the retraction material ,the corresponding comprecap was placed on to the abutment to push the material deep into the gingival sulcus. After 4 min, the comprecap with the set retraction material attached to it was removed from the patient mouth.
the cord packed into the gingival sulcus around the tooth
used directly in the tray