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Pain,swelling and quality of life assessment in the patients who underwent extraction of impacted third molars followed by application of gel containing amino acid and hyaluronic acid or normal saline.

Clinical evaluation and quality of life assessment after removal of impacted third molar followed by intra-alveolar application of gel containing amino acid and sodium hyaluronate Vs. normal saline â?? A double blinded randomized split mouth study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/031834
Enrollment
16
Registered
2021-03-09
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K011- Impacted teeth

Interventions

Intervention1: intra-alveolar application of 2ml topical gel after the extraction of impacted third molar: Surgical extraction of impacted tooth will be done first it will take 15-20 mins. Followed b

Sponsors

All India Institute of medical Sciences New delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age between 18 to 29 years. 2.ASA I and II patients. 3.Patients having bilateral symmetrical mesioangular impacted lower third molar â?? Similar surgical difficulty.

Exclusion criteria

Exclusion criteria: 1.Patients having acute signs of infection like pain, trismus, cellulitis, space infection. 2.Impacted tooth having Active caries and Periodontal diseases. 3.Patients having impacted tooth with periapical bony changes. 4.Patients give a history of antibiotic or anti-inflammatory drug consumption for the past 7 to 14 days (depends on the drug). 5.Patients having any medical co-morbidity, especially uncontrolled DM and Bleeding disorder. 6.Patients taking systemic corticosteroids, immunosuppressive agents, bisphosphonates, or cancer chemotherapeutic agents. 7.Patients with oral submucous fibrosis and radiation-induced fibrosis. 8.Pregnancy ladies. 9.Patient having allergy/ adverse drug reaction to any medications. 10.Patient refusing to give consent.

Design outcomes

Primary

MeasureTime frame
Pain - the level of pain will be assessed using 10-point visual analogue scale (VAS)Timepoint: Post operative day 1,3,7,14—

Secondary

MeasureTime frame
post-operative complications like suture site dehiscence, pus discharge, dry socketTimepoint: Post operative day 1,3,7,14;Quality of life assessment using OHIP-14 QuestionnaireTimepoint: Post operative day 1,3,7,14;Swelling â?? Measured using Modified Gabka and Matsumara methodTimepoint: Post operative day 1,3,7,14;Trismus â?? Interincisial mouth opening was recorded using rigid straight ruler.Timepoint: Post operative day 1,3,7,14—

Countries

India

Contacts

Public ContactDr SARAVANAN L

All India Institute of Medical Sciences, New Delhi

ajoyroy@hotmail.com011-26542329

Outcome results

None listed

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