Clinical Trials Logo

Analgesia clinical trials

View clinical trials related to Analgesia.

Filter by:

NCT ID: NCT04264689 Completed - Analgesia Clinical Trials

Perioperative Thoracotomy Analgesia; Different Analgesic Modalities

Start date: March 2, 2020
Phase: N/A
Study type: Interventional

the study aim is to compare the analgesic effect of thoracic epidural versus serratus plane block versus erector spinae block in thoracic surgeries

NCT ID: NCT04259502 Not yet recruiting - Analgesia Clinical Trials

Rhomboid Intercostal Block vs Erector Spina Plan Block for Peri-operative Analgesia in Mastectomy

Start date: February 2020
Phase: N/A
Study type: Interventional

Effectiveness of erector spinae plane block for analgesia in breast surgery was documented in previous studies. Rhomboid intercostal block may be beneficial for analgesia in breast surgery. The aim of this study is to compare the peri-operative analgesic effect of rhomboid intercostal block with erector spinae plane block in mastectomy operation. This trial was designed as prospective randomized single-blind study. The included patients will be assigned into two groups: RIB-Group where the patients will receive ultrasound-guided rhomboid intercostal block and ESP-Group where the patients will receive ultrasound-guided erector spinae plane block prior to the operation. Primary outcome will be peri-operative pain scores and secondary outcomes will be peri-operative opioid consumption and peri-operative hemodynamic effect of these blocks.

NCT ID: NCT04257695 Completed - Chronic Pain Clinical Trials

Developing and Pilot Testing an Opioid Tapering Protocol

TapPro
Start date: May 4, 2021
Phase: N/A
Study type: Interventional

This study proposes to pilot test an intervention to facilitate opioid pain reliever (OPR) tapering in primary care. The intervention will incorporate a clinician embedded within primary care to follow tapering dose schedules to support providers as well to deliver a psychosocial curriculum to support and engage patients. In a pilot randomized controlled trial (RCT), the study will examine the preliminary efficacy and feasibility of the manualized, protocol-based tapering intervention ("TapPro") compared to usual care. As there is no standard definition or outcome for tapering, the primary efficacy outcome is a decrease in OPR dose over six months. Separately, the study proposes a clinically meaningful dose reduction (greater than or equal to 30 percent) as a secondary outcome. The central hypotheses' are that a tapering intervention with patient and provider support is feasible in a primary care setting and can result in greater dose reduction when compared to usual care.

NCT ID: NCT04252313 Recruiting - Analgesia Clinical Trials

Music as Analgesia During Neonatal Circumcision

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

Neonatal circumcision is one of the most frequently performed and more painful procedures. Sharara et al (2017) showed the combination of EMLA + Sucrose + Ring Block provides the highest standard of pain management. A combination which has been adopted by practitioners who perform circumcisions at the normal nursery at AUBMC. An element which is overlooked in its ability to enhance or suppress stress and consequently pain is sound/noise, music. The specific aim of this study is to test the added effectiveness of music (Group B: intervention) to the established standard for analgesia [EMLA + Sucrose + Ring Block] (Group A: control) in further managing the pain of newborn males undergoing circumcision.

NCT ID: NCT04251819 Active, not recruiting - Analgesia Clinical Trials

Buprenorphine Plus Baclofen to Increase Analgesia in Healthy Volunteers

Start date: January 21, 2021
Phase: Phase 2/Phase 3
Study type: Interventional

To determine if baclofen will enhance buprenorphine analgesia for acute pain in healthy volunteers.

NCT ID: NCT04250272 Recruiting - Lung Cancer Clinical Trials

Serratus Anterior Plane Block Versus Intercostal Nerve Block for Postoperative Analgesia

Start date: August 16, 2019
Phase: N/A
Study type: Interventional

A prospective randomized controlled study was undertaken to compare the postoperative analgesic effect between ultrasound-guided serratus anterior plane block and intercostal nerve block after video-assisted thoracoscopic lobectomy.

NCT ID: NCT04248608 Completed - Analgesia Clinical Trials

Perioperative Analgesic Modalities for Breast Cancer Surgeries

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

The incidence of breast cancer is among women world wide, detection increased with introduction of mammography as a screening tool. surgical resection of breast cancer contributes to the generation of acute and chronic post mastectomy pain. This study aims at comparing the effect of erector spinae block versus serratus block versus intravenous morphine in patients undergoing modified radical mastectomy for breast cancer surgeries regarding pain control and possible side effects

NCT ID: NCT04246697 Completed - Clinical trials for Head and Neck Cancer

Multimodal Pain Study in Free Flap Patients

Start date: November 1, 2019
Phase: Phase 4
Study type: Interventional

This study will be fashioned as a randomized, prospective study comparing Pain Management Arm A and Pain Management Arm B. Arm A will have scheduled Tylenol with opioids available as needed (PRN) in the peri-operative period. Arm B will undergo scheduled Gabapentin, Ketorolac and Tylenol as well as the Anesthesiology team managing regional nerve blocks, with opioids available PRN in the peri-operative period. The amount of pain medication used by all patients will be recorded as well as pain scores documented on a pain scale (0-10 with 0 indicating no pain and 10 indicating worst pain ever) as well as ABC pain scale throughout the patients' hospital stay. Morphine equivalents for the opioids will be calculated for each arm while observing pain scores. Then, the investigators will compare these two groups to see if there is a difference in opioid pain medication used. The study team's hypothesis is that the use of Gabapentin, Ketorolac, and Tylenol in combination will significantly reduce (at least 30% of Mean Morphine Equivalents - MME) the use of opioid medication for patients undergoing head and neck free flap reconstruction with similar to improved pain scores.

NCT ID: NCT04238572 Completed - Analgesia Clinical Trials

Evaluation of Immersive Audiovisual Distraction Impact on Peroperative Opioid Consumption.

AmbuCineView
Start date: February 19, 2020
Phase: N/A
Study type: Interventional

This study evaluate the impact of an audiovisual distraction device on the peroperative opioid consumption for outpatient procedures with Remifentanil added to local anesthesia. Half of patients will receive an audiovisual distraction device while the other half not.

NCT ID: NCT04236674 Recruiting - Pain Clinical Trials

Thermomechanical Distraction and Social Anesthesia in Interventional Radiology to Improve Patient Satisfaction

Start date: January 27, 2020
Phase: N/A
Study type: Interventional

The study will prospectively analyze the analgesic and anxiolytic effects of thermomechanical stimulation (cold and vibration effects) with or without patient selected music preference during non-sedating interventional radiology procedures.