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Pain Management clinical trials

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NCT ID: NCT03990922 Completed - Pain Management Clinical Trials

CTPVB for Hepatectomy

Start date: June 20, 2019
Phase: N/A
Study type: Interventional

Moderate to severe postoperative pain often influence patients quality of recovery after hepatectomy. Systemic opioids given with patient-controlled analgesia has been used after hepatectomy in many medical center, but the analgesic effect can be limited and undesirable side effects may bring about negative effects on patients recovery. Regional block has been proved to improve patients postoperative recovery in many kinds of surgeries. The investigators therefore designed a prospective, randomized, subject and assessor blinded, parallel-group, placebo controlled study to test the hypothesis that continuous right thoracic paravertebral block increase patients quality of recovery score on the 7th postoperative day after hepatectomy in patients receiving i.v. patient-controlled analgesia (PCA) with morphine.

NCT ID: NCT03982784 Completed - Pain Management Clinical Trials

TQLB for Postoperative Pain After Laparoscopic Partial Nephrectomy

Start date: June 10, 2019
Phase: N/A
Study type: Interventional

This prospective, randomized study,control study aims to compare the analgesic effect,opioids consumption,quality of recovery,length of hospital stay,et al. between single-injection QLB(quadratus lumborum block)+ intravenous patient-controlled analgesia (IPCA) and intravenous patient-controlled analgesia (IPCA) alone in patients undergoing laparoscopic partial nephrectomy.

NCT ID: NCT03942237 Completed - Pain Management Clinical Trials

Transmuscular Quadratus Lumborum Block for Postoperative Pain After Laparoscopic Adrenalectomy

Start date: May 10, 2019
Phase: N/A
Study type: Interventional

This prospective, randomized control study aims to compare the analgesic effect, satisfaction with anesthesia and analgesia between single-injection QLB (quadratus lumborum block)+general anesthesia (GA) and general anesthesia (GA) alone in patients undergoing laparoscopic adrenalectomy.

NCT ID: NCT03933124 Completed - Pain Clinical Trials

The Effect of Virtual Reality on Post-surgical Pain and Recovery.

VIRTUAL
Start date: May 21, 2019
Phase: N/A
Study type: Interventional

This study evaluates the effect of Virtual Reality (VR) on pain and recovery in 100 post-operative patients. 60 patients will be included in the intervention group; they will use VR minimal 3 times a day on day 2-4 after surgery, on the surgical ward, as an add-on intervention next to standard care. 40 patients in the control group will only receive standard postoperative care.

NCT ID: NCT03916835 Completed - Pain Management Clinical Trials

MUSIDORE PED Study

MUSIDORE
Start date: May 28, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to measure the efficacy of music during a painful procedure in pediatric intensive care unit. Music therapy has real effects on the pain level already proven in adults units. Our objective is to apply this technic to children. The investigators will evaluate this technic during cleaning care which is daily procedure for each stable patient and wich may be painful in this population.

NCT ID: NCT03903172 Completed - Pain Management Clinical Trials

Post-partum Non-pharmacologic Pain Management

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

This study aims to examine whether use of an abdominal binder for postpartum patients after vaginal delivery can effectively manage their pain and reduce the need for pharmacologic analgesics. The investigators hypothesize that use of an abdominal binder will decrease patient pain as reported on a visual analog scale of one to ten, and will decrease quantity of pain medications given. The study will be conducted at the Berry Women's Center at Miami Valley Hospital. Potential eligible participants will be approached regarding the study on admission to labor and delivery. The investigators will recruit 130 participants that will be randomized to two study arms, standard care and standard care plus abdominal binder with 65 participants in each study arm. Data will be collected prospectively while participants are admitted, and through review of electronic medical records. Potential benefits of this study include investigation of a cost-effective method for pain management that could improve patient comfort and reduce need for medications.

NCT ID: NCT03887650 Completed - Pain Management Clinical Trials

LIBERATE - LIposomal Bupivacaine vERsus Adjuncts in Total shouldErs

Start date: March 11, 2019
Phase: Phase 4
Study type: Interventional

This will be a single-center, prospective, randomized controlled cross-sectional study comparing interscalene brachial plexus block with liposomal bupivacaine versus bupivacaine with epinephrine and PF dexamethasone in patients undergoing primary shoulder arthroplasty. Primary endpoint will be total opioid consumption in the first three post-operative days.

NCT ID: NCT03868787 Completed - Pain Management Clinical Trials

Transcutaneous Electrical Nerve Stimulation (TENS) for Pain Control During Cervical Dilator Placement Prior to Dilation and Evacuation

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

This study evaluates the use of Transcutaneous Electrical Nerve Stimulation (TENS) as a method of pain control during osmotic dilator insertion prior to dilation and evacuation. Half the group will have an active TENS unit and half will have a sham or placebo TENS unit.

NCT ID: NCT03853694 Completed - Pain Management Clinical Trials

Efficacy and Safety of EXPAREL Versus Standard of Care (SoC) in Subjects Undergoing Elective Cesarean Section

CHOICE
Start date: March 4, 2019
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare total opioid consumption by subjects in different treatment groups. Another purpose of this study is to assess how well EXPAREL works, collect any safety data and assess your satisfaction using EXPAREL.

NCT ID: NCT03757715 Completed - Pain Management Clinical Trials

Regional Anesthesia to Reduce Opioid Use Following Functional Endoscopic Sinus Surgery

Start date: May 20, 2019
Phase: Phase 4
Study type: Interventional

Opioids are prescribed for moderate to severe pain disorders; however, there are contraindications and side effects that are common to all opioids. The investigators hypothesize using regional anesthetic during sinus surgery will reduce surgical pain, therefore decreasing the need for post-operative opioid medication. The primary of objective is to determine if a long-acting local regional anesthetic applied during a surgery will reduce post-operative oral opioid usage.