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The effect of Geltamp on teeth extraction complications

Evaluation of Gelatamp effectivness on pain and bleeding after teeth extraction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015113025303N1
Enrollment
71
Registered
2015-12-30
Start date
2015-12-06
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Bleeding. Condition 2: Pain. Haemorrhage NOS Acute pain

Interventions

Intervention 1: Intervention group: Using of one Geltamp in dental socket after tooth extraction Gelatamp is made of 95% foam gelatin sponge and 5% finely dispersed colloidal silver. In this study wil
Prevention
Intervention group: Using of one Geltamp in dental socket after tooth extraction Gelatamp is made of 95% foam gelatin sponge and 5% finely dispersed colloidal silver. In this study will use Gelatamp m
Control group: Using of routine dressing with sterile gauze after tooth extraction

Sponsors

Vice Chancellor for research of Qom University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age between 20-45 years; No sensitivity to silver; Not using corticosteroid; antibiotic and anticoagulant within the past month; Not having clotting disorder; No acute or uncontrolled infection at the surgery site; No malignancy at the surgery site; No history of exposure of surgery site to radiation; Not using contraceptive drug over the past month; Not smoking; Not having hypertension, diabetes, thyroid disorder and blood disorder. Exclusion criteria: No readmission for second tooth extraction; Failure to complete postoperative; Using of out of prescription drugs; Discontinuation of participation in the study; Developing a systemic disease.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bleeding. Timepoint: Every Five Minutes until Stop of Bleeding. Method of measurement: Minute by Timer.

Secondary

MeasureTime frame
Pain. Timepoint: Every Six Hour for 48 Hour. Method of measurement: Visual Analog Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPooya Piri

Qom University of Medical Sciences

dr_pooyapiri@yahoo.com+98 25 3770 3738

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026