Effect of Acupressure on Postoperative Pain With Gynecologıcal Surgery

Status Active, not recruiting

Clinical Trial Summary

Clinical Trial Description

In this study, the effect of acupressure on postoperative pain level in women with abdominal gynecologıcal surgery will be studied and it will be conducted as a randomized controlled intervention study to examine the relationships with each other.The sample group will consist of 102 women, 51 in the intervention group and 51 in the control group.Within the scope of the study, the data will be collected using the 'Personal Information Form and Short-Form McGill Pain Questionnaire(SF-MPQ)' created by the researcher. Data will be obtained by the researcher by faceto-face interviews with women. In addition, women in the intervention group will receive acupressure once on postoperative days 0 and 1. Acupressure points related to gynecological surgery (large intestine (LI4), stomach (ST36) and spleen (SP6)) will be applied for a total of 12 minutes with 2 minutes of pressure on each point. Women in the control group will continue their routine care. Data will be evaluated with SPSS-26 package. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06172439
Study type	Interventional
Source	Saglik Bilimleri Universitesi
Contact
Status	Active, not recruiting
Phase	N/A
Start date	June 1, 2023
Completion date	January 30, 2024

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT05619796` - Assessment of Clinical & Radiographic Efficiency of Manual & Pediatric Rotary Systems in Primary Root Canal Preparation	N/A
Recruiting	`NCT05338671` - Effect of Post-Operative Anesthetics on Post-Operative Pain in Patients Receiving Endodontic Treatment	Phase 4
Completed	`NCT05593341` - Opioid Education in Total Knee Arthroplasty	N/A
Completed	`NCT05584696` - Effectiveness of Green Color Exposure on Dental Anxiety	N/A
Not yet recruiting	`NCT05255146` - Cryoanalgesia and Post-thoracotomy Pain in Minimally Invasive Cardiothoracic Surgery	N/A
Not yet recruiting	`NCT06020196` - The Safety and Efficacy of Surgical Rectus Sheath Block for Postoperative Analgesia After Elective Cesarean Delivery	N/A
Completed	`NCT01697748` - Prospective Study on Cesarean Wound Outcomes	N/A
Completed	`NCT01681966` - A Single-dose Open-Label Study to Assess the Safety and Preliminary Efficacy of PRF 110 in Open Herniorrhaphy Surgery	Phase 2
Completed	`NCT01442818` - Patient Satisfaction and Pain Control Following Reconstructive Vaginal Surgery	N/A
Completed	`NCT00625911` - Ketamine Improves Post-Thoracotomy Analgesia	N/A
Terminated	`NCT05494125` - Effects of Continuous ESP Catheters on Recovery, Pain and Opioid Consumption After Multilevel Spine Surgery	N/A
Recruiting	`NCT04767399` - Comparison of Postoperative Pain After Instrumentation in Different Visits With Different Single File Systems.	N/A
Not yet recruiting	`NCT05863624` - Open and Endoscopic Technique in Female Inguinal Hernia Repair. FemaleHernia	N/A
Completed	`NCT06048744` - Ultrasound Guided Erector Spinae Plane Block vs External Oblique Intercostal Plane Block for Nephrectomy	N/A
Active, not recruiting	`NCT05374499` - Double-Blinded Randomized Controlled Study Investigating the Efficacy of Exparel (Liposomal Bupivacaine) for Postoperative Pain Relief in Mandibular Third Molar Extractions	Phase 4
Completed	`NCT05510947` - Acute Postoperative Pain and Catastrophizing in Patients Undergoing Unicompartmental Knee Arthroplasty
Completed	`NCT06082479` - The Effect of Intra Oral Cryotherapy in Patients With Symptomatic Apical Periodontitis	N/A
Completed	`NCT05552391` - Dexametomedine Versus Ketamine as an Adjuvant in Erector Spinae Block for Perioperative Thoracotomy Pain Control	Phase 4
Completed	`NCT06065683` - Acute Postoperative Pain Prevalence and Intensity in the First 72 Hours
Recruiting	`NCT04909060` - Does the Newborn Infant Parasympathetic Evaluation (NIPE) Index Predict Postsurgical Pain in Children