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NCT ID: NCT06243302 Active, not recruiting - Anal Fistula Clinical Trials

Anal Fistulae Internal Opening Closure by OTSC Clip After Video Assisted Tract Fulguration

VAAFT-OTSC
Start date: September 2014
Phase:
Study type: Observational [Patient Registry]

This study is expected to recruit 20-25 cases treated with video assisted anal fistula treatment. Additionally the internal opening of the fistulae will be closed by an OTSC clip.

NCT ID: NCT06243224 Completed - Hypertension Clinical Trials

The Effect Of High Intensity Interval Training And Moderate Intensity Continuous Training In Patients With Hypertension

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

Comparison of high intensity interval training (HIIT) and moderate intensity continuous training (MICT) in patients with hypertension patient in terms of aerobic capacity, blood pressure level, anxiety and depression scores, quality of life, kinesiophobia levels and sleep quality measurement.

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: NCT06242587 Active, not recruiting - Coccyx Injury Clinical Trials

Impar VS Coccygeal Block in the Treatment of Coccidine

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

The aim of this study was to evaluate the efficacy of coccygeal nerve blockade. Impar sympathetic ganglion blockade is a common treatment method used in coccygeal pain. However, experience with the coccygeal nerve is scarce in the literature. The investigator planned to follow up coccidynia patients who underwent impar sympathetic ganglion blockade and coccygeal nerve blockade for 3 months after the procedure. The investigator's aim is to compare the efficacy of coccygeal nerve blockade with impar blockade.

NCT ID: NCT06242431 Recruiting - Clinical trials for Postoperative;Pain Management

Effects of Serratus Posterior Superior Intercostal Plane Block and Pectoralis Nerve Block in Coronary Artery Surgery

Start date: February 7, 2024
Phase: N/A
Study type: Interventional

Postoperative analgesia is a critical risk factor for the development of pulmonary and cardiovascular complications in all types of chest surgery, particularly coronary artery bypass graft (CABG) surgery. Patients with high levels of pain who cannot breathe effectively may experience atelectasis, cardiac ischemia, and arrhythmias. This prolongs hospitalization and increases the frequency of postoperative pulmonary complications and morbidity. If postoperative acute pain is not adequately treated, it may lead to the development of chronic pain, hindering patients from recovering normal activities for an extended period. In addition to medications, various neuroaxial and peripheral nerve blocks can be used in cardiac surgery. The use of high-dose heparin during surgery, along with neuroaxial anesthesia (thoracic epidural and intrathecal opioids), is controversial. Thoracic paravertebral block (TPVB) has demonstrated efficacy and is considered a method with fewer potential side effects compared to thoracic epidural anesthesia. However, TPVB has become less preferred in cardiac surgery due to its sympathetic blockade. Recently, peripheral nerve blocks have gained popularity as alternatives. These blocks include pectoralis nerve blocks (PECS-I, PECS-II), serratus anterior plane block (SAPB), serratus posterior superior intercostal plane block (SPSIPB), erector spinae plane block (ESPB), transverse thoracic plane blocks (TTMP), pectointercostal-fascial blocks (PIF), and intercostal nerve blocks. These blocks are newer and more superficially located compared to TPVB. Additionally, these fascial blocks are considered safer in terms of side effects as they do not cause sympathetic blockade like TPVB. The hypothesis of this study is that SPSIPB can provide more extensive dermatomal analgesia compared to PECS-II, resulting in more effective postoperative analgesia. Therefore, this study plans to compare the analgesic effects of ultrasound-guided SPSIPB and PECS-II block applications in patients undergoing coronary artery bypass surgery with sternotomy.

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: NCT06242028 Active, not recruiting - Postoperative Pain Clinical Trials

Comparison of the Effects of Perineural Dexamethasone and Systemic Dexamethasone in PENG Block

Start date: December 27, 2023
Phase:
Study type: Observational

Hip fractures are morbid conditions, especially in elderly patients, and their treatment is usually surgical. Pericapsular nerve group block targets the hip capsule. The aim of this study is to investigate and compare the perioperative analgesic efficacy of PENG blocks applied investigation of the effect of perinuerally and systemic dexamethasone on pain scores in the first 24 hours of PENG block in patients undergoing hip fracture surgery under spinal anesthesia.