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Effects of the Elements clinical trials

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NCT ID: NCT05445362 Completed - Clinical trials for Effects of the Elements

Efficacy of Diode Laser in Maturogenesis of Immature Teeth With Necrotic Pulps

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

Recruited patients with immature permanent maxillary anterior teeth with non-vital pulp, and periapical radiolucency, age ranging from 8 to16 years old were randomly allocated into three groups (n=13): Group I, disinfected using the triple antibiotic paste, Group II, disinfection was done using diode laser, and Group III, were disinfected using the triple antibiotic paste, diode laser was used for biostimulation. All groups were evaluated for the increase in root length and thickness and decrease in apical diameter at baseline, 3, 6, 9, and 12 months after treatment

NCT ID: NCT05100615 Recruiting - Clinical trials for Effects of the Elements

Healing Assessment of Osseous Defects After Surgical Removal of Periapical Lesions

Start date: November 2021
Phase: N/A
Study type: Interventional

recruited patients with periapical lesions will be divided into three groups and surgically treated with three types of bone graft (hydroxyappatite, nanohydroxyappatite and PRF WITH NANOHYDROXTAPPATITE) and then evaluated for month, three months and six months for the healing of periapical bone

NCT ID: NCT04761211 Completed - Clinical trials for Effects of the Elements

Effect and Safety of Smart Bra (PUMCH)

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

This is a multicenter, prospective clinical study was conducted to evaluate the safety and effectiveness of Xiehe smart bra for breast disease screening in outpatients with breast surgery. According to the patients' wishes and written informed consent, they were randomly assigned to the study group. A total of 2000 patients were expected to be enrolled. The training group: validation group = 1:1.

NCT ID: NCT04607018 Completed - Clinical trials for Effects of the Elements

Effect PMA-Zeolite on the Mineral Metabolism and Blood Parameters (MMBP Study)

Start date: November 17, 2015
Phase: N/A
Study type: Interventional

The Panaceo Micro Activation (PMA) -zeolite s a certified medical device throughout the European Union and absorbs defined harmful substances (mainly heavy metals and ammonium ions) in the gastrointestinal tract, while at the same time the alkaline ions contained in the crystal lattice are released (Mg2+, Ca2+, K+, Na+). Through a recent study the main-effect of zeolite was defined (support/ strengthen the intestinal wall barrier) and as a side-effect the measurement of the mineral metabolism was included, without documenting any significant changes. Its potential in releasing minerals needs to be investigated further to broaden the knowledge from previous study-outcomes as described. Broadening this knowledge through measuring defined blood-parameters was the aim of this human trial.

NCT ID: NCT04338633 Recruiting - Clinical trials for Effects of the Elements

Post-operative Pain Reduction

Start date: April 2020
Phase: N/A
Study type: Interventional

Recruited patients with necrotic pulp after application of conventional calcium hydroxide paste are assigned to group, Calcium hydroxide nanoparticle group and Combined Calcium hydroxide with silver nanoparticle group and record postoperative pain afterwards.

NCT ID: NCT04327453 Recruiting - Clinical trials for Effects of the Elements

Effect of Removal of Double Antibiotic Paste on Post Operative Pain

Start date: April 2020
Phase: N/A
Study type: Interventional

Recruited patients with necrotic pulp after application of double antibiotic paste are assigned to group (XP Endo Finisher file) and group( Passive ultrasonic irrigation) and group (conventional syringe irrigation with side vented needle) to remove intracanal medication and record postoperative pain afterwards.

NCT ID: NCT04324086 Recruiting - Clinical trials for Effects of the Elements

Effect of Removal of Intracanal Medication on Post Operative Pain

Start date: April 1, 2020
Phase: N/A
Study type: Interventional

Recruited patients with necrotic pulp after application of Calcium hydroxide are assigned to group (XP Endo Finisher file) and group( Passive ultrasonic irrigation) and group (conventional syringe irrigation with side vented needle) to remove intracanal medication and record postoperative pain afterwards.