2 registrations that name aloe Vera as a study arm and are recruiting or about to, as ClinicalTrials.gov listed them on Oct 20, 2026. Read each listing for its full criteria and current status.
Kymata never assesses eligibility. Each listing names its own criteria; only its study team can say whether someone can join. Trial doses are given under the trial's monitoring and are not a schedule for anyone outside it.
Filter 2 registrations
Status
All 2 registrations
Not yet recruitingNCT07084194
Impact of Integrating Two Nano Based Irrigants With Two Activation Techniques in Treatment of Teeth With Acute Pulpitis on Postoperative Pain and Flare up Incidence
No phase
Minia University
About 64 people
Starts Sep 10, 2025 (estimated)
In plain words A study of aloe Vera in people of any age, run by Minia University. It plans to enroll about 64 people and lists no sites yet.
Who it lists and where
Who the trial lists, as registered
Lists people of any age; healthy volunteers accepted. Conditions: Postoperative Pain; Flare up; Flare Up, Symptom.
Age 18-60 (adults only)
multiple-rooted with multiple root canal.
Permanent teeth with mature apex and complete root formation.
Without root caries.
6 more inclusion criteria and the exclusion criteria are on the listing.
This study aimed to evaluate and compare impact of integrating passive ultrasonic activation and laser activation with nano-chitosan and aloe vera in terms of postoperative pain and flare-up incidence in a randomized clinical trial.
Where, as registered
No sites listed yet.
Not yet recruitingNCT05223127
Aloe Vera on Caesarean Section Wound
No phase
KTO Karatay University
About 60 people
Starts Aug 1, 2024 (estimated)
In plain words A study of aloe Vera in female participants 18 to 35, run by KTO Karatay University. It plans to enroll about 60 people and lists no sites yet.
1 more inclusion criterion and the exclusion criteria are on the listing.
What it tests, as registered
Aloe vera
Registered summary
Conducting clinical research in line with the literature recommendation, with a method that is low-cost, accessible, easy-to-use, and examined in an evidence-based design related to cesarean section wound, which negatively affects the quality of life of women in the postpartum period, constitutes the original value and our main motivation of the project.