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NCT ID: NCT06243055 Completed - Obesity Clinical Trials

Reliability and Validity of the Turkish Version of the Laval

Start date: November 15, 2021
Phase:
Study type: Observational

The study is a Turkish validity and reliability study of the Laval questionnaire.

NCT ID: NCT06242886 Completed - Breastfeeding Clinical Trials

After Caesarean Section Oxitocin Breast Massage Anthropometric Characteristics of the Newborn

OM
Start date: February 20, 2023
Phase: N/A
Study type: Interventional

Background: Delays in breastfeeding and milk release after cesarean section may negatively affect the early initiation of breastfeeding and the mother's breastfeeding self-efficacy. Research Aims: The aim of this study was to investigate the effect of breast and oxytocin massage after cesarean section on the anthropometric characteristics of the newborn and breastfeeding self-efficacy. Methods: The study was conducted in a single-blind randomized controlled type and 126 mothers who delivered by cesarean section in the postpartum department of a private hospital in Istanbul/Turkey were randomized into three groups as 42 breast massage, 42 oxytocin massage and 42 control group.

NCT ID: NCT06242639 Completed - Clinical trials for Survival, Prosthesis

Metal-ceramic Fixed Partial Dentures Fabricated With Laser Sintering

Start date: June 1, 2021
Phase:
Study type: Observational

The aim of this retrospective clinical study was to evaluate the clinical acceptability of metal-ceramic fixed partial dentures (FPD) manufactured utilizing direct metal laser-sintering technology, taking into account the short-term, medium-term, and long-term outcomes. The Federation Dentaire International (FDI) World Dental Federation criteria were used to evaluate the esthetic, functional, and biological clinical acceptability of the patients who met the inclusion criteria

NCT ID: NCT06242340 Completed - Baths Clinical Trials

The Effect of Newborn's First Bath Time on Physiological Variables

Start date: October 18, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to examine the effect of the first bath timing after birth on the physiological variables of the newborn and to determine the correct bath time. 1. H₁: There is a difference in the effect of bathing preterm newborns after 24 hours or 48 hours on the peak heart rate. 2. H2: There is a difference in the effect of bathing early term newborns after 24 hours or 48 hours on the peak heart rate. 3. H3: There is a difference in the effect of bathing preterm newborns after 24 hours or 48 hours on their respiratory rate. 4. H4: There is a difference in the effect of bathing early term newborns after 24 hours or 48 hours on their respiratory rate. 5. H5: There is a difference in the effect of baths given to preterm newborns after 24 hours or 48 hours on body temperature. 6. H6: There is a difference in the effect of baths given to early term newborns after 24 hours or after 48 hours on body temperature. 7. H7: There is a difference in the effect of baths given to preterm newborns after 24 hours or 48 hours on oxygen saturation. 8. H8: There is a difference in the effect of baths given to early term newborns after 24 hours or after 48 hours on oxygen saturation.

NCT ID: NCT06242314 Completed - Palate; Wound Clinical Trials

L-PRF Versus A-PRF on Palatal Wound Healing

Start date: January 10, 2021
Phase: N/A
Study type: Interventional

Different approaches are used to reduce post-operative complications associated with the palatal wound site after free gingival graft (FGG) harvesting. The aim of this study was to compare the effects of L-PRF and A-PRF on palatal wound healing after free gingival graft harvesting and patients' quality of life.

NCT ID: NCT06241690 Completed - Child, Only Clinical Trials

Cold Applications on the Pain Level of Children With Sutures

Start date: November 11, 2021
Phase: N/A
Study type: Interventional

Purpose:This research was conducted as an experimental study with pretest and posttest control groups in order to evaluate the effect of post-suture cold applications on the pain level of children with sutures. Design and Methods: This study is a randomised controlled study. In the study, there were 150 children in the experimental group and 150 children in the control group.

NCT ID: NCT06241443 Completed - Childbirth Problems Clinical Trials

Nursing Students & Positive Birth Perception & Simulation

Start date: September 20, 2022
Phase: N/A
Study type: Interventional

The study aimed to investigate the impact of simulation-based training on nursing students' perception of positive birth and natural birthing approaches.

NCT ID: NCT06240793 Completed - Pain, Chronic Clinical Trials

Comparison of Unilateral and Bilateral Transforaminal Epidural Steroid Injection

Start date: June 15, 2023
Phase: N/A
Study type: Interventional

Lumbar radicular pain affects the person's quality of life. The most common cause of lumbar radicular pain is disc herniation. In radicular pain due to lumbar disc herniation, epidural steroid injections are frequently applied to patients who do not benefit from medical treatment and physical medicine modalities. Epidural steroid injection inhibits the synthesis and release of pro-inflammatory substances that develop as a result of mechanical compression.In the transforaminal epidural technique, the solution is administered to the anterior epidural space and spreads to the ipsilateral periradicular area. The applied solution does not cross the midline and there is no contralateral drug spread. Although bilateral transforaminal epidural steroid injection is recommended in unilateral lumbosacral disc herniation because the inflammation is bilateral, unilateral transforaminal steroid injection has been applied in most studies. We aimed to to evaluate the effects of unilateral and bilateral transforaminal epidural steroid injection on pain intensity, functionality and medication use in unilateral lumbosacral disc herniation

NCT ID: NCT06240507 Completed - Plantar Fascitis Clinical Trials

Posterior Tibial Nerve PRF vs Intralesional RFT for Painful Calcaneal Spur and Plantar Fasciitis

Start date: January 2, 2023
Phase: N/A
Study type: Interventional

This study aims to compare the efficacy of ultrasound (US)-guided posterior tibial nerve pulsed radiofrequency (PTN PRF) and fluoroscopy (FL)-guided intralesional radiofrequency thermocoagulation (RFT) for the treatment of painful calcaneal spur and plantar fasciitis refractory to conservative treatments. For this evaluation, a numerical rating (NRS) and the American Orthopedic Foot and Ankle Society (AOFAS) ankle hindfoot scores will be used before and after both interventions.

NCT ID: NCT06240494 Completed - Clinical trials for Trigeminal Neuralgia

Predictive Factors in Maxillary and Mandibular Nerve Radiofrequency Treatment for Trigeminal Neuralgia

Start date: September 1, 2022
Phase:
Study type: Observational

Trigeminal neuralgia is one of the most common craniofacial neuralgias and one of the most severe types of facial pain, typically limited to the distribution of the trigeminal nerve. The first-line treatment for trigeminal neuralgia is medical therapy and primarily antiepileptic drugs. Various interventional and surgical methods can be used in patients who do not respond to medical treatment or who cannot tolerate side effects. Pulsed radiofrequency treatment of maxillary and mandibular nerves may provide longer-lasting pain relief in trigeminal neuralgia.This study aimed to investigate the clinical and demographic characteristics affecting treatment success in patients who underwent ultrasound-guided pulsed radiofrequency of the maxillary and/or mandibular nerves for trigeminal neuralgia.