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Assessing the Effectiveness of Aqua Titan Patch in Reducing Postoperative Complications After Wisdom Tooth Surgery: A Randomized Control Trial

EVALUATION OF EFFICACY OF AQUA TITAN PATCH IN POSTOPERATIVE SEQUELAE AFTER IMPACTED MANDIBULAR THIRD MOLAR SURGERY – A RANDOMIZED CONTROL TRIAL - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076441
Enrollment
44
Registered
2024-11-08
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: Z768- Persons encountering health services in other specified circumstances

Interventions

Intervention1: aqua titan patch: aqua titan patch will be used to rule out the efficacy in post operative pain, swelling and trismus after impacted mandibular third molar surgery Control Interventio

Sponsors

Geetanjali Dental & Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients between age of 18-45 years of both genders. 2. Patients indicated for surgical removal of impacted mandibular third molar. 3. Healthy patients falling under ASA I and ASA II 4. Subjects able and willing to provide written informed consent and compliant with study procedure.

Exclusion criteria

Exclusion criteria: 1. Patients with mouth opening less than 30mm. 2. Patient with allergy with NSAIDS. 3. Patients having history of drug abuse. 4. Patients having any systemic or local immunodeficiency. 5.Patient is under regular analgesics and anti-depressants. •Having any blood coagulation impairment. •Presence of any acute oral infection. •Have been suffering with uncontrolled diabetes or other systemic diseases. •Having previous history of radiation therapy in the head and neck region. •Pregnant and nursing women. •Soft tissue impactions.

Design outcomes

Primary

MeasureTime frame
Pain Swelling TrismusTimepoint: all these parameters will be measured on 1st, 3rd and 7th post operative day

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Shallu Bansal

Geetanjali Dental and Research Insitute

drshallu23@gmail.com9116155666

Outcome results

None listed

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