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Evaluation the Effects of Echium Amoenum Tea on Pain Control after Clinical Crown lengthening Surgery

Evaluation the Effects of Echium Amoenum Tea on Pain Control after Clinical Crown lengthening Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180630040290N3
Enrollment
50
Registered
2019-07-30
Start date
2019-07-11
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Decrease the crown length of the tooth. Loss of teeth due to accident, extraction or local periodontal disease

Interventions

Intervention 1: Intervention group: The intervention group 24 hours before surgery every 12 hours once , and one hour before the start of surgery, will use a dose of Echium Amoenum Tea. Intervention 2

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Having conscious awareness Patients who are candidates for surgery can increase the length of the crown of the tooth (in the posterior maxilla). ages from 20 to 65 years old Patients who are physically and mentally healthy Patients with moderate to severe periodontitis at the same depth of envelope

Exclusion criteria

Exclusion criteria: Patients with systemic or mental illness Alcoholism or any psychoactive substance Sensitization known to be NSAID, caffeine or acetaminophen Having any bleeding disorder Patients at risk for any post-surgical infection Patients with liver problems Patients with a heart and blood pressure problems Persons with mental and physical disabilities (persons who do not have the competence to satisfy their personal satisfaction and complete the questionnaires) Patients who use of Echium Amoenum Tea are risky for them Patients who need to increase the dose of sedative or injectable forms of sedative Patients with no needs for bone surgery

Design outcomes

Primary

MeasureTime frame
Extent of pain in the operated part. Timepoint: ?After 30 minutes, 1 and 3 hours after the operation , 1 and 2 and 3 days after the operation. Method of measurement: En 30 minutes, 1 and 3 hours after the operation by VAS(Visual Analogue Scale) , after 1 and 2 and 3 days by VRS(Verbal Rating Scale).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir reza Babaloo

Tabriz University of Medical Sciences

amirezababaloo@yahoo.com+98 41 3335 5921

Outcome results

None listed

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