Clinical Trials Logo

Postoperative Pain clinical trials

View clinical trials related to Postoperative Pain.

Filter by:

NCT ID: NCT04959825 Completed - Postoperative Pain Clinical Trials

The Role of Preoperative Melatonin in Reducing the Inhaled Isoflurane Requirements in Open Nephrectomy

Start date: July 15, 2021
Phase: Early Phase 1
Study type: Interventional

Melatonin is a hormone that the pineal gland in the brain produces. Melatonin fulfills many functions in the body but it is mostly known for maintaining a circadian rhythm that is governed by the central circadian pacemaker (biological clock) in the suprachiasmatic nuclei in the hypothalamus. Melatonin works by attaching to receptors or nerve endings in the suprachiasmatic nucleus (SCN) in the hypothalamus. It binds to melatonin receptor 1 and melatonin receptor 2, commonly referred to as MT1 and MT2. People can take it as a natural or synthetic supplement to promote restful sleep. Melatonin showed promise for preventing shifts in sleep and wake times in people with jetlag and improving sleep in people with insomnia. It can also be used for headaches, cancer, and Alzheimer's disease. Melatonin can be used as an analgesic, sedative, and hypnotic drug that can distinguish it as an attractive alternative premedicant

NCT ID: NCT04950491 Completed - Quality of Life Clinical Trials

Patient-reported Outcome Measures Comparing Static Computer-aided Implant Surgery and Conventional Implant Surgery

Start date: July 9, 2019
Phase: N/A
Study type: Interventional

The aim of this randomized controlled trial was to compare PROMs in patients receiving single tooth replacement in posterior sites by s-CAIS and CIS.

NCT ID: NCT04947345 Not yet recruiting - Postoperative Pain Clinical Trials

The Availability and Safety Study of Remimazolam Besylate for Injection on Sedation of ERAS Patients

Start date: September 1, 2021
Phase: Phase 3
Study type: Interventional

This trial intends to evaluate Remimazolam Besylate's availability and safety compared with propofol.

NCT ID: NCT04943549 Completed - Postoperative Pain Clinical Trials

Erector Spinae Plane Block Impact on Quality of Recovery After Lumbar Spinal Decompression

ESPB
Start date: June 1, 2021
Phase: Phase 4
Study type: Interventional

Erector spinae plane block (ESPB) as a new trunk fascia block technique was proposed in 2016. ESPB has aroused the interest of many nerve block experts. The benefits of ESPB are not yet demonstrated. The specific mechanism is still controversial. Some believe that ESPB can block the posterior root of the spinal nerve and produce part of the para-spinal block effect with the diffusion of the drug solution. The present study will carried out to compare the performance of the erector spinae plane block combined with general anesthesia in addicts versus non addicts' patients regarding the local analgesic effect, recovery after surgery and side effects.

NCT ID: NCT04938882 Completed - Postoperative Pain Clinical Trials

Effect of Transversus Abdominis Plane Block With Compound Lidocaine on Pain After Gynecological Surgery

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

Purpose: To explore effects of ultrasound-guided transversus abdominis plane block with compound lidocaine on postoperative pain after gynecological laparotomy.

NCT ID: NCT04935723 Completed - Anxiety Clinical Trials

The Effects of Reiki on Abdominal Surgery Patients' Anxiety, Fear, Postoperative Pain and Life Findings

Start date: June 15, 2020
Phase: N/A
Study type: Interventional

Abdominal surgeries are those in which pain is felt severely due to the incision close to the diaphragm and an intensive neural network in the abdominal area. If the patient's post-operative pain is not controlled; Since it will restrict patient mobility, it can cause problems on many systems such as the pulmonary, cardiovascular and neuroendocrine system, and even suppress the immune system. Surgical intervention decision can cause anxiety in individuals regardless of the type of surgical procedure. Fear of anesthesia, fear of death, possibility of developing complications after surgery, pain, change in daily life activities, loss of social life and loss of control can lead to anxiety. In addition to all these, factors such as pain, fear, anxiety that stimulate the sympathetic nervous system can increase the pulse rate, blood pressure and respiratory rate. Reiki, a complementary and alternative medicine (TAT) method, is a bioenergy based on the energy use of the body and has been used in various cultures for centuries in preventing and treating some diseases. Reiki is thought to help balance the body's natural energetic systems and reduce anxiety by transferring the available energy through hands. During Reiki, the activity of the parasympathetic system increases, pain and anxiety decrease. Thus, the patient's complaints are reduced by providing early discharge with possible complications after surgery. Studies on the effectiveness of reiki, which is increasing worldwide use and recommended as a treatment approach for health services, are insufficient. The aim of this study, which is planned as a three-group interventional randomized control, is to examine the effect of reiki application on patients' negative reflections on pain, anxiety, fear and vital signs, which is the major surgery type in which patients experience the most pain.

NCT ID: NCT04928521 Completed - Postoperative Pain Clinical Trials

Erector Spinae Plane (ESP) Block With 20 ml Versus 30 ml in Cardiac Surgery

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

Even though erector spinae plane (ESP) block is shown to be efficient in cardiac surgery, it is still controversial how much volume is necessary for efficient analgesic effect for sternotomy and drain tube pain relief. This study aims to investigate the optimal local anesthetic volume (20 mL versus 30 mL) with ESP block for open-heart cardiac surgery.

NCT ID: NCT04920669 Completed - Postoperative Pain Clinical Trials

Dexmedetomidine in Erector Spinae Block in Postoperative Analgesia

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

60 female patients scheduled for breast cancer surgeries, allocated in 3 groups for erector spinae block with bupivacaine and erector spinae block with dexmedetomidine added to bupivacaine and control group. During anesthesia: total intraoperative fentanyl required will be recorded. After surgery the first time of request for analgesic will be recorded. after request of analgesia all patients will be connected to PCA device containing morphine solution, the amount of morphine consumed during the first 24 hours will be recorded.

NCT ID: NCT04917510 Not yet recruiting - Postoperative Pain Clinical Trials

Evaluating the Efficacy of Erector Spinae Block in Routine Hip Arthroscopy

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

The aim of this project is to evaluate the efficacy of preoperative erector spinae blocks in arthroscopic hip surgery. This will be a prospective randomized controlled trial.

NCT ID: NCT04915534 Completed - Postoperative Pain Clinical Trials

Gender Specific Differences in Postoperative Sore Throat for Ambu® AuraGain™ Laryngeal Mask

LadyLAMA
Start date: December 6, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate gender specific risk factors and the influence of cuff pressure in the occurrence of postoperative sore throat and hoarseness following general anaesthesia using Ambu® AuraGain™ Laryngeal Mask.