A clinical study to know the effect of various cold therapy applications on after treatment oral health related quality of life in patients with symptomatic irreversible pulpitis
- Conditions
- Health Condition 1: K040- Pulpitis
- Registration Number
- CTRI/2021/05/033365
- Lead Sponsor
- Dr veluru jyothshna
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Patients with symptomatic irreversible pulpitis with apical periodontitis.
2.Patients of age group between 18-50 yrs.
3.Patients who will show prolonged response even after the removal of the stimulus.
4.Patients will be included in the study after evaluation of electric pulp testing response.
5.Patient who has the ability to understand the use of OHIP-14 and pain questionnaires will be provided informed consent for endodontic treatment
1.Patients with immature teeth, sinus tract, periapical abscess or facial cellulitis.
2.Patients with generalised attrition.
3.Patients with Re -RCT will be excluded.
4.Patient with known allergies, or any contra-indication to opioid or non-opioid analgesics including aspirin or NSAIDs.
5.Patients with known allergy to local anaesthesia, sodium hypochlorite and chlorhexidine.
6.Presence of systemic diseases like cardiovascular disease, renal disease, bleeding disorders or any anti-coagulant use with in last month.
7.Pregnant and lactating mothers.
8.Patients under pain medication for dental or any other illness within 24 hours.
9.Patients who are unable or unwilling to complete the OHIP-14 and pain questionnaires.
10.Patients who are unwilling to sign consent for endodontic treatment.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment of Oral health related quality of life using Oral Health Impact Profile -14 (OHIP 14) questionnaireTimepoint: At 72hours post-operatively
- Secondary Outcome Measures
Name Time Method Assessment of pain using modified verbal descriptive scale(MVDS)Timepoint: At 72hours post-operatively