- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07598188
Evaluation of Post Operative Pain After Using Intracranial Cryotherapy During Single Visit RCT
Evaluation of Post Operative Pain After Using Intracranial Cryotherapy During Single Visit Root Canal Treatment in Teeth With Symptomatic Apical Periodontitis
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Objective:
To compare the reduction in post operative pain of treatment group with control group using normal; saline at room temperature at 24 and 48 hours
Methodology:
A total of 60 patients presenting with single-rooted teeth exhibiting symptomatic apical periodontitis were subjected to a randomized allocation into two groups of 30 each. Irrigation was done using 3% sodium hypochlorite for 5 seconds in all 60 teeth. Group 1 underwent final irrigation utilizing normal saline at room temperature. Group 2 received final irrigation using normal saline refrigerated between 2-5°C. Pain levels were assessed and recorded before the procedure and at 24 and 48-hour time intervals.
Statistical analysis:
Statistical packages for the Social Sciences (SPSS) Version 22 will be used for data analysis. Mean and SD and Frequencies will be used for quantitative variables (Age and pain), and frequency and percentage for qualitative variable (gender). The continuous variable pain score will be compared among control and cryotherapy group by using independent sample t test. Effect modifiers ( age and gender) will be stratified by using post stratified independent sample t test .The P value < 0.05 will be considered as the threshold for statistical significance, at a confidence interval of 95%.
Studietyp
Inskrivning (Beräknad)
Fas
- Inte tillämpbar
Kontakter och platser
Studiekontakt
- Namn: Aroosa Bakhtawar, BDS
- Telefonnummer: 03379248459
- E-post: bakhtawararoosa@gmail.com
Studera Kontakt Backup
- Namn: Saima Azam, BDS, FCPS
- Telefonnummer: 00923005350740
- E-post: saima.azam@iideas.edu.pk
Studieorter
-
-
Federal
-
Islamabad, Federal, Pakistan, 44000
- Islamabad Dental Hospital
-
Kontakt:
- Aroosa Bakhtawar, BDS
- Telefonnummer: 03379248459
- E-post: bakhtawararoosa@gmail.com
-
Kontakt:
- Saima Azam, BDS, FCPS
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Beskrivning
Inclusion Criteria:
Individual (male/female) with age >18 years with symptomatic apical periodontitis in permanent teeth
Exclusion Criteria:
- Teeth with calcified canals or aberrant root anatomy,
- Female Pregnant patients
- Patients using medications such as analgesics or anti-biotics drugs and
- Those who refuse to participate in the study
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Sekventiell tilldelning
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Intervention Group
In the cryotherapy group, following completion of biomechanical preparation, the root canals will be irrigated with 20ml of 0.9% physiological saline solution at a temperature of 1.5-2.5°C
for 5 min
|
In this study participant are suing 0.9% normal saline but the temperature will be different for both groups .In cryotherapy group participant are using saline at cold temperature1.5-2.5°C
|
|
Inget ingripande: Control Group
In the control group, final irrigation will be performed using 20 mL of 0.9% physiological saline solution at room temperature for 5 min
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
To evaluate the reduction of postoperative pain
Tidsram: 24-48 hours
|
Patients will be instructed to record their pain score on VAS at 24 and 48 h. and will be asked to contact and visit in case they experience severe pain.
If visit is not possible,a telephonic feedback will be recorded and assistance will be guided
|
24-48 hours
|
Samarbetspartners och utredare
Studieavstämningsdatum
Studera stora datum
Studiestart (Beräknad)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- IslamabadDentalHospital(IDH)
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Studerar en amerikansk FDA-reglerad produktprodukt
produkt tillverkad i och exporterad från U.S.A.
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .