Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

Comparison of Quadro-Iliac Plane Block and Transversalis Fascia Plane Block for Open Inguinal Hernia Repair

This prospective observational cohort study aims to compare the postoperative analgesic effectiveness of the quadro-iliac plane block (QIPB) and transversalis fascia plane block (TFPB) in patients undergoing elective unilateral open inguinal hernia repair under spinal anesthesia. The choice of block technique will be determined by the attending anesthesiologist as part of routine clinical practice, independently of study participation, and no randomization or study-directed assignment will be performed. Patients receiving QIPB or TFPB will be prospectively followed as two cohorts. Postoperative pain scores at rest and during coughing will be assessed at 2, 4, 6, 12, and 24 hours. Time to first rescue analgesic requirement, rescue tramadol use, block performance time, and adverse events will also be compared between the two cohorts.

Participants needed: 80
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Vezirköprü State HospitalUpdated: Oct 7, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Age between 18 and 75 years. [+4]

Refusal to participate in the study. [+7]

Status: Not yet recruiting

Comparison of TLIP Block and QIP Block for Postoperative Analgesia After Lumbar Spine Surgery

This study compares two regional anesthesia techniques used for pain control after lumbar spine surgery: the classic thoracolumbar interfascial plane (TLIP) block and the quadratus lumborum-iliac plane (QIP) block. Patients between 18 and 65 years of age who undergo elective lumbar discectomy (up to two spinal levels) will be observed based on which block their treating anesthesiologist chooses to use as part of routine clinical practice. No randomization or additional intervention beyond standard care will be performed. Researchers will record the total amount of opioid pain medication used in the first 24 hours after surgery, the time until the first request for pain medication, pain scores at several time points after surgery (0, 1, 2, 4, 8, 12, and 24 hours), and any side effects (such as nausea, vomiting, or sedation) or complications related to the block. The aim is to compare the effectiveness and safety of these two techniques in reducing pain and opioid use after lumbar spine surgery.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Vezirköprü State HospitalUpdated: Aug 6, 2026Locations: 1
Eligibility criteria

Aged 18-65 years [+3]

Hypersensitivity or allergy to study medications [+10]