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Postoperative Pain clinical trials

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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: NCT03623399 Recruiting - Postoperative Pain Clinical Trials

Laparoscopic Gas Pressure and Postoperative Pain Score

Start date: August 7, 2018
Phase: N/A
Study type: Interventional

Aim of the study is to determine the effect of different laparoscopic intraoperative intraabdominal gas (CO2) pressures on the extent of postoperative pain scores.

NCT ID: NCT03622489 Recruiting - Postoperative Pain Clinical Trials

Comparing Protocols for Analgesia Following Elective Cesarean Section

Start date: March 1, 2017
Phase: Phase 4
Study type: Interventional

Women undergoing elective cesarian section will be assigned to 3 groups for postoperative analgesia: 1. Scheduled doses of IV acetaminophen + PO Ibuprofen 2. Scheduled doses of PO acetaminophen + PO Ibuprofen 3. "On demand" doses of acetaminophen, dipyrone and ibuprofen.

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: NCT03619447 Not yet recruiting - Postoperative Pain Clinical Trials

Comparison of ESP Block Versus Serratus Block

Start date: September 15, 2018
Phase: Phase 4
Study type: Interventional

Total 60 patients, American society of anaesthesiology physical status I-II aged between 18-65 who underwent totally mastectomy will recruit to the study. The patients randomly divided into two groups. Ultrasound guided Erector spinae plane block (ESP) will perform with 15 ml bupivacaine+ 5 ml lidocaine in Group ESP and ultrasound guided serratus anterior plane (SAP) block will perform with 5 ml bupivacaine+ 5 ml lidocaine in Group SAP. Postoperative pain assessment will apply with 11-point numerical rating scale (NRS) and postoperative analgesic requirement will calculate and record with morphine consumption (patient controlled analgesia).

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.

NCT ID: NCT03604068 Recruiting - Postoperative Pain Clinical Trials

Pulsed Short Wave Therapy In Cesarean Section

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

This clinical study is designed to assesses the benefit of adding pulsed shortwave therapy to the postoperative pain and recovery protocol following Cesarean section. Pulsed shortwave therapy is a safe adjunct pain therapy for acute and chronic pain.

NCT ID: NCT03602664 Recruiting - Postoperative Pain Clinical Trials

Postoperative Recovery After Thoracic Surgery

POLO
Start date: June 5, 2018
Phase:
Study type: Observational

A questionaire specifically developed using in depth interviews with patients that has undergone surgery has been developed. This questionaire will be used for longterm follow in patients undergoing thoracic surgery. 200 patients will be asked to fill in this questionaire preoperatively as well as 3 and 12 months after surgery to assess symptomburden after surgery with specific aim to study postoperative pain as well as other physical, mental and cognitive problems that may affect the patient and their daily activities, health, return to work, family life and economy.

NCT ID: NCT03601780 Not yet recruiting - Postoperative Pain Clinical Trials

Local Wound Infiltration in Renal Surgery

Start date: August 2018
Phase: Phase 2
Study type: Interventional

Multimodal analgesia is a rational approach to treat various components of postoperative pain.