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Postoperative Pain clinical trials

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NCT ID: NCT05893771 Completed - Postoperative Pain Clinical Trials

Depomedrol for Genicular Nerve Block.

Start date: June 7, 2023
Phase: N/A
Study type: Interventional

This study is designed to test the efficacy of adding Depomedrol a long-acting steroid to bupivacaine for relieving postoperative pain and reducing opioid requirements following total knee replacement surgery. For this purpose, Depomedrol will be added to bupivacaine for ultrasound-guided Genicular nerve block combined with spinal anesthesia.

NCT ID: NCT05890079 Completed - Postoperative Pain Clinical Trials

External Oblique Intercostal Plane Block for Liver Transplantation Donors

Start date: May 8, 2023
Phase: N/A
Study type: Interventional

Postoperative pain management is one of the important factors to improve rehabilitation and enhance recovery. External oblique intercostal plane block may be used for abdominal wall analgesia to provide effective analgesia for abdominal surgery. The aim of this study is to investigate the postoperative analgesic efficacy of external oblique intercostal plane block and subcostal transversus abdominis plane block in living liver donors. Researchers will compare the external oblique intercostal plane block group with subcostal transversus abdominis plane block to see if the external oblique intercostal plane block is effective for postoperative analgesia in living liver donors.

NCT ID: NCT05880732 Completed - Postoperative Pain Clinical Trials

Magnesium Sulfate on Postoperative Pain

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

Breast cancer is the most diagnosed type of cancer in women in Turkey and in the world. According to the World Health Organization data, the rate of newly diagnosed breast cancer was reported as 11.6% in 20181. Acute postoperative pain occurs in 40% of patients undergoing surgery for breast cancer2. In the early postoperative period, opioids are commonly used analgesics in the treatment of pain, but they have various side effects such as gastrointestinal, urinary and respiratory symptoms3. Non-opioid analgesics can be used to reduce opioid use and thus limit its side effects. Magnesium sulfate (MgSO4) is an N-Methyl D-Aspartate (NMDA) receptor antagonist that has been used for postoperative analgesia and reducing both the duration and intensity of pain by preventing central sensitization in response to peripheral painful stimulus4-9. The primary aim of this study is to investigate the postoperative analgesic efficacy of MgSO4 in patients who were scheduled for mastectomy with the diagnosis of breast cancer. The secondary aim of our study is to evaluate the changes in perioperative vital signs that may occur due to MgSO4.

NCT ID: NCT05854537 Completed - Postoperative Pain Clinical Trials

Sphenopalatine Ganglion Block in Maxillofacial Surgeries

Start date: March 20, 2023
Phase: N/A
Study type: Interventional

Patients will be divided into 2 groups, 30 each. Group A will receive sphenopalatine ganglion block via a gauze soaked in local anesthetic introduced in the 2 nostrils then by local anesthetic injected by a cannula into both nostrils. Group B will undergo the same procedure, but normal saline will be used instead of the local anesthetic.

NCT ID: NCT05853133 Completed - Postoperative Pain Clinical Trials

Evaluation of Postoperative Quality of Recovery Score in Radical Prostatectomy With Erector Spinae Plane Block

Start date: May 16, 2023
Phase: N/A
Study type: Interventional

Radical prostatectomy is performed with a median incision below the umbilicus. Although the position is supine, the waist extension movement is created in order to facilitate access to the surgical site. The investigator think that this may be a factor affecting the postoperative comfort, not only in the pain in the surgical field, but especially in patients with low back pain (facet joint pain, etc.). Techniques that provide quality postoperative recovery with reduced morbidity and rapid return to daily activities are important for anesthesiologists. In this study, the investigator aimed to evaluate the postoperative recovery quality (Quality of Recovery score (QoR-40)) of patients who underwent open radical prostatectomy and underwent erector spina plan block and wound infiltration for postoperative analgesia.

NCT ID: NCT05841693 Completed - Quality of Life Clinical Trials

Quality of Recovery in Parturients Consumed Preoperative Carbohydrate Fluid for Elective Cesarean Delivery

QoR-10
Start date: May 12, 2023
Phase: Phase 4
Study type: Interventional

The establishment of the Enhanced Recovery After Cesarean protocols resulted in to the production of specific care pathways with the aim of optimizing recovery after cesarean delivery (CD) and to reduce the costs to the health care system. Carbohydrate rich fluids are offered in this aspect to enhance postoperative quality of recovery. The primary aim of this randomised control trial is to assess the impact of pre-operative carbohydrate loading on obstetric quality of recovery after elective cesarean section.

NCT ID: NCT05840419 Completed - Surgery Clinical Trials

Retrospective Comparison Between AirSeal® and Standard Insufflation in Appendicular Peritonitis

APPAS
Start date: January 1, 2022
Phase:
Study type: Observational

The AirSeal System Valve-less Trocar is known to decrease postoperative pain, consumption of analgesics, operating time, and length of stay in adults during robotic and laparoscopic procedures. The investigators would like to know if these allegations also apply to children.

NCT ID: NCT05834023 Completed - Postoperative Pain Clinical Trials

Bupivacaine Versus Bupivacaine Plus Lidocaine in Infraclavicular Block

Start date: May 2, 2023
Phase: Phase 4
Study type: Interventional

In this study, the investigators will compare two different anesthetic solutions in the infraclavicular block in patients having forearm, wrist, and hand surgery. The solutions will be bupivacaine 0.5% versus bupivacaine 0.25% plus lidocaine 1%, both associated with epinephrine 5 mcg/ml and dexamethasone 4 mg. The main objective of this investigation is to demonstrate that using higher concentrations of bupivacaine alone results in a significant block duration increase compared with the mixture of bupivacaine and lidocaine.

NCT ID: NCT05831761 Completed - Postoperative Pain Clinical Trials

Effectivness of Tramadol or Topic Lidocaine on Postoperative Analgesia in Laparoscopic Colorectal Resection.

Start date: September 1, 2009
Phase: N/A
Study type: Interventional

Comparison of different postoperative analgesia after laparoscopic colorectal surgery

NCT ID: NCT05826093 Completed - Postoperative Pain Clinical Trials

Cutaneous Sensory Block Area of the Subcostal Ultrasound-Guided Transversus Abdominis Plane Block

CUSBAT
Start date: February 15, 2022
Phase:
Study type: Observational

Patients planned for elective laparoscopic cholecystectomy received a peroperative ultrasound-guided subcostal transversus abdominis plane block (USTAP) at the beginning of the procedure. At T90 minutes after the end of anaesthesia the cutaneous sensory block area (CSBA) was measured using cold sensation and mapped with a sterile marker. The CSBA was photodocumented and the area calculated.