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Pain, Acute clinical trials

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NCT ID: NCT05103800 Completed - Pain, Acute Clinical Trials

Investigation of the Effect of White Noise Listening on Pain and Comfort During Invasive Interventions in Newborns

IEWNLPCDIIN
Start date: November 15, 2021
Phase: N/A
Study type: Interventional

Comfort, distress and the absence of pain can be described as free from anxiety, somewhat enjoyable and ease (peaceful) situation. The child health and disease nurse should come up with physiological problems of the baby, increase the comfort degree to reduce the stress level of the baby and ensure improvement in the baby's location. This research was experimentally designed to investigate the effect of the baby's own intrauterine heart sound on pain and comfort during the invasive procedures applied to the healthy born babies in the delivery units of the Batman Gynecology and Pediatrics Hospital. The research will be performed by selecting samples in a simple random sampling method from the babies who born healthy and timely in the normal vaginal way. The number of samples will be determined by power analysis method after pilot study. The previously white noise will have listened to the babies in experimental group and will be recorded by camera during invasive interventions and the pain and comfort scale will be applied. The scales will be applied to the control group let them without listening White noise but also will be recorded with camera and thus the data will be collected. A nurse working in the unit will perform invasive interventions, later two specialists will watch video records and so the pain and comfort scales will be filled. No study on this subject was found in the international literature review. Based on the need to fill this gap in the literature, it seems that the study will contribute to the field of child health and diseases nursing.

NCT ID: NCT05079594 Completed - Pain, Acute Clinical Trials

The Effects of Auditory Interventions on Comfort and Mothers' Anxiety in Newborns

Start date: March 15, 2021
Phase: N/A
Study type: Interventional

The heel blood procedure for newborn screening is done for almost all babies within the first 48 hours of birth. It is stated that non-pharmacological methods in reducing pain during the heel blood collection process are simple, effective, free, and very cost-effective. Studies have shown that auditory interventions (such as mother's voice, white noise) used in invasive procedures distract the infant and create a cognitive strategy for pain control. According to this information, one aim of the study is to determine the effect of the mother's voice and white noise, which are non-pharmacological methods, on the comfort level of the baby in the heel blood procedure. It is thought that especially acute painful procedures applied to infants will reduce the level of stress and anxiety in parents. Another aim of this study is to determine the effect of a mother's voice and white noise, which are non-pharmacological methods, on the state anxiety levels of mothers in the heel blood collection process.

NCT ID: NCT05069350 Completed - Pain, Acute Clinical Trials

Bupivacaine vs Oxybuprocaine Topical Anesthesia in IVI

Start date: September 1, 2021
Phase: Early Phase 1
Study type: Interventional

comparing two local anaesthetic agents, Bupivacaine 0.5% versus Oxybuprocaine used topically to provide surface anaesthesia before IVI procedures.

NCT ID: NCT05068245 Completed - Anxiety Clinical Trials

Music to Reduce Patient Reported Pain During Intrauterine Device (IUD) Placement in the Office

MIUD
Start date: August 28, 2020
Phase: N/A
Study type: Interventional

This study seeks to determine if music reduces pain and anxiety in comparison to routine pain control measures alone during insertion of intrauterine contraceptive devices (Mirena, Paragard)

NCT ID: NCT05064072 Completed - Pain, Acute Clinical Trials

Pain Felt During Removal of the Products From Infant's Skin Used in Nasogastric Tube Fixation

Start date: July 1, 2021
Phase: N/A
Study type: Interventional

The present study was planned to evaluate the pain of 4-6 weeks infants felt during removal of the adhesive products from newborn's skin used in the fixation of nasogastric tube in neonatal and infant units. The hypothesis of the study is "Water-based barrier tape is more effective to reduce pain than hydrocolloid barrier tape.

NCT ID: NCT05049577 Completed - Analgesia Clinical Trials

Preanesthetic Analgesia/Nociception Index (ANI) and Propofol Injection Pain

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

Recently, Analgesia Nociception Index (ANI) has been evaluated for objectively measuring peri-operative pain and to guide intra-operative opioid administration during various surgeries. Propofol injection pain (PIP) is a common problem and can be very distressing to the patient.

NCT ID: NCT05005871 Completed - Pain, Postoperative Clinical Trials

Comparison of Quadratus Lumborum Intramuscular and Transmuscular in Postoperative Pain

Start date: September 1, 2021
Phase: N/A
Study type: Interventional

Acute pain is reported in approximately 80% of patients undergoing postoperative care for various types of surgical procedures in the United States. Another study reported patient postoperative pain intensity with 75% with severe pain in the first 1 to 2 postoperative days and 38% reporting moderate to severe pain at 14 postoperative days. Several modalities have been used as the standard for the management of pain postoperative C-sections. One of the postoperative analgesic modalities for SC is quadratus lumborum block (QLB). This technique has advantages in relieving postoperative pain after C-section because it is considered to be able to relieve visceral pain as well as somatic pain. The transmuscular QLB (QLBT) approach is one of the most frequently used. This technique was found to be effective with regard to the distribution of analgesics to the paravertebral spaces which is the hallmark of QLB. However, this technique was found to be difficult to perform. Difficulties were reported related to the position of the procedure i.e. lateral or sitting position.

NCT ID: NCT04997434 Completed - Pain, Acute Clinical Trials

Impact of Modern Art Therapy on Patients' Anxiety and Pain During the Waiting Time in an Emergency Department

Start date: August 1, 2021
Phase: N/A
Study type: Interventional

The primary objective of this study is to investigate whether, during a waiting period in an emergency department, the patient's participation in a modern art therapy session decreases the patient's level of anxiety and pain. As a secondary objective, this study aims to explore whether participation in a modern art therapy session is perceived positively by the patient. This objective will be assessed by both patient self-report and art therapist heteroreport. In this work, the investigators will therefore seek to demonstrate the potential positive impact of modern art therapy conducted during times of waiting for examination or results.

NCT ID: NCT04978532 Completed - Pain, Acute Clinical Trials

Effect of Guided Imagery Method on Procedural Pain in Children

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

The study was conducted as a randomized controlled experimental trial. The children who attended a pediatric surgical clinic for venipuncture divided into two groups via randomization in the computer environment. After the randomization, the children in the guided imagery group listened to a voice recording prepared in a studio during venipuncture. This voice recording named 'Stroll in the Forest' helped the children to imagine that they are strolling in a forest and guided them. On the other hand, no application was performed on the children in the control group during the venipuncture. The primary outcome of the study was pain and secondary outcomes were heart rate and oxygen saturation values. The pain was evaluated by the children, parents, and observer. The pulse and oxygen saturation values were measured before, during, and after the venipuncture.

NCT ID: NCT04953182 Completed - Pain, Acute Clinical Trials

Pain Modality Treatment After Hemorrhoidectomy

Start date: July 1, 2016
Phase:
Study type: Observational

Hemorrhoidectomy is one of the operations that causes the greatest intensity of pain. Treatment of postoperative pain is essential for the well-being of the patient. Long-term use of opioids and different drugs can have unintended consequences. The objective is to corroborate which pain treatment modality is better in patients after hemorrhoidectomy.