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Postoperative Pain clinical trials

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NCT ID: NCT03650998 Completed - Postoperative Pain Clinical Trials

Transmuscular Quadratus Lumborum Block for Total Laparoscopic Hysterectomy.

Start date: September 28, 2018
Phase: Phase 4
Study type: Interventional

Study is designed to assess the effect of the transmuscular quadratus lumborum block on postoperative opioid consumption and pain for patients undergoing laparoscopic hysterectomy. Study is randomized, placebo-controlled and blinded. Seventy patients will be included.

NCT ID: NCT03644147 Completed - Postoperative Pain Clinical Trials

Additive Effect of Intravenous Acetaminophen on Postoperative Pain Control

Start date: August 27, 2018
Phase: N/A
Study type: Interventional

This study aimed to evaluate the additive effect of acetaminophen on postoperative pain control in patients receiving nefopam and fentanyl-based patient-controlled analgesia. Participants undergoing laparoscopic hysterectomy will be randomly assigned to treatment group or control group. After end of surgery, acetaminophen or normal saline (placebo) will be administered intravenously depending on the group assigned.

NCT ID: NCT03640390 Completed - Postoperative Pain Clinical Trials

Dexmedetomidine Versus Magnesium Sulfate Infusion During Spinal Anesthesia

Start date: August 30, 2018
Phase: Phase 3
Study type: Interventional

The aim of this work is to compare the hemodynamic and analgesic properties of Dexmedetomidine and Magnesium sulphate infusion in lower abdominal surgery.

NCT ID: NCT03639389 Completed - Postoperative Pain Clinical Trials

Postoperative Pain, Recovery and Discharge Following Robot-assisted Laparoscopic Prostatectomy

RAPID
Start date: January 1, 2019
Phase: Phase 3
Study type: Interventional

Prostate cancer is the commonest cancer form in men in Northern Europe. Management of the cancer often includes surgical removal of the primary tumor. In the last 5-10 years, robot assisted laparoscopic prostatectomy (RALP) has become common. Good pain relief is central to early mobilization and greater patient satisfaction. Randomized controlled studies on pain relief following RALP are few and the role of spinal analgesia in pain management following robotic surgery has not been described. Techniques available for pain relief following RALP include spinal anesthesia with or without opiates, intravenous analgesia with morphine or a multimodal pain management technique using a combination of several analgesics. Spinal anesthesia and analgesia reduces the surgical stress and inflammatory response following laparoscopic colorectal surgery and may offer similar benefit even during RALP. Early perioperative complications may cause postoperative morbidity following robotic surgery, and sometimes delay home discharge. Since all robotic operations in the pelvic region are performed in a deep Trendelenberg position, this can even have negative consequences for the heart, brain and the lungs. Cardiac complications in the form of minimal cardiac injury or mild heart failure have not been previously studied following RALP. Additionally, patients are sometimes delirious in the early postoperative period following RALP. The precise cause for this remains unclear and may be related to pain, cognitive dysfunction or an urge to pass urine despite a urinary catheter. In addition to good postoperative pain relief, early postoperative mobilization and home discharge are important milestones in recovery of full function following major surgery. With improvement in surgical technique, the time has come to evaluate if RALP can be performed on an ambulatory basis. The main aims of this study are: 1. Can RALP be performed on an ambulatory basis and patients ready to be discharged home at 8 pm? 2. To determine if spinal anesthesia reduces pre-discharge pain intensity, stress response and other perioperative side effects. 3. Is sufentanil or fentanyl the analgesic of choice when administered spinally together with bupivacaine as an analgesic. 4. To determine the frequency and severity of cardiac and respiratory complications in the steep Trendelenberg position during RALP. 5. To assess the quality of recovery, quality of life and activities of daily living following ambulatory RALP?

NCT ID: NCT03638960 Completed - Postoperative Pain Clinical Trials

Interscalene Single Shot With Plain Bupivacaine Versus Liposomal Bupivacaine for Arthroscopic Shoulder Surgery

Start date: February 21, 2019
Phase: Phase 4
Study type: Interventional

The investigators will be comparing pain scores and opioid use in patients receiving interscalene peripheral blocks with plain bupivacaine versus those receiving liposomal bupivacaine. Liposomal bupivacaine is described as releasing local anesthetic up to 72 hours after its injection; therefore if liposomal bupivacaine can provide extended pain relief compared to plain bupivacaine, the investigators can consider using it as our primary local anesthetic. As secondary outcomes, the investigators will also be looking at difference in functional status and long-term differences between the two local anesthetics.

NCT ID: NCT03628950 Completed - Postoperative Pain Clinical Trials

Interscalene Versus Combined Infraclavicular-suprascapular Nerve Blocks

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

The aim of this trial is to compare the analgesic efficiency and hemi-diaphragmatic paralysis of the standard ultrasound-guided interscalene (ISB) brachial plexus block with the combined use of costoclavicular approach of infraclavicular brachial plexus block and suprascapular nerve block (ICB-SSB) for patients undergoing arthroscopic rotator cuff repair. Authors hypothesize that the combined use of ICB-SSB could lead to equivalent postoperative analgesic effect to the standard ISB with less hemi-diaphragmatic paralysis.

NCT ID: NCT03626753 Completed - Postoperative Pain Clinical Trials

Comparison of Two Routes of Administration of a Multimodal Analgesic Protocol in Postoperative Cesarean Section

Start date: January 1, 2015
Phase: Phase 2/Phase 3
Study type: Interventional

Many drugs with various mechanisms of action are used for postcaesarean pain relief. Although the response to pain relief is sometimes believed to be individual, it is very important to establish the most effective with the least adverse effects type of oral analgesia for women after caesarean section. Optimal pain control post-caesarean section will benefit not only the mother and her baby, but also a healthcare system. Optimal pain control may shorten the time spent in hospital after caesarean section and, therefore, reduce healthcare costs.

NCT ID: NCT03621345 Completed - Postoperative Pain Clinical Trials

Bilateral Ultrasound-Guided Erector Spinae Plane Block For Postoperative Analgesia in Breast Reduction Surgery

Start date: August 15, 2018
Phase: N/A
Study type: Interventional

Erector spinae plane (ESP) block is a novel block developed by Forero to treat severe neuropathic pain and was firstly reported in 2016. Anatomical and radiological investigations in fresh cadavers indicate that its site of action is likely at the dorsal and ventral rami of the thoracic spinal nerves. The ESP block has a clear and simple sonoanatomy, it is easy to perform, not time consuming and generally well tolerated by the patients. So, the investigators believed that the ESP block may be an effective and safer alternative to paravertebral block, epidural analgesia and other myofascial thoracic wall blocks in breast surgery and designed a prospective, randomised, placebo-controlled trial for pain management.

NCT ID: NCT03620591 Completed - Postoperative Pain Clinical Trials

Lidocaine and Analgesia After Laparoscopic Cholecystectomy

Start date: July 2, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate how effective is the intraoperative use of lidocaine to attenuate postoperative pain and opioids consumption after laparoscopic cholecystectomy

NCT ID: NCT03612947 Completed - Postoperative Pain Clinical Trials

TAP Block in Laparoscopic Cholecystectomy.

Start date: September 3, 2018
Phase: Phase 2
Study type: Interventional

Ultrasound-guided transversus abdominis plane block is now widely used in abdominal surgery. Recently, magnesium sulphate is used as adjuvant to local anesthetics.