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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05253300
Other study ID # SRPShoulderPain
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 14, 2021
Est. completion date July 24, 2021

Study information

Verified date February 2022
Source Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was carried out to determine the effect of placing the semi-recumbent position in reducing pain in patients who developed shoulder pain after laparoscopic cholecystectomy. HO: The application of the semi-recumbent position to patients who develop shoulder pain after laparoscopic cholecystectomy has no effect on reducing pain. H1: The application of semi-recumbent position in patients who develop shoulder pain after laparoscopic cholecystectomy has an effect on reducing pain.


Description:

In addition to pharmacological interventions for the relief of postoperative complications such as pain in patients undergoing laparoscopic cholecystectomy, non-pharmacological applications; It is evaluated that it will be beneficial in increasing patient satisfaction, reducing the need for analgesic drugs, reducing the cost of hospitalization due to the side effects of drugs and increasing the quality of care. With the results of this research, it is evaluated that the effect of positioning, which is one of the independent activities of nurses who base their care on evidence-based practices, on pain will be beneficial to increase the evidence-based nursing knowledge in the literature.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date July 24, 2021
Est. primary completion date July 24, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Those who had surgery with laparoscopic cholecystectomy - Those between the ages of 18-65, - Patients in ASA I-II group - Patients undergoing general anesthesia Exclusion Criteria: - Epidural analgesia after surgery - Patients with reactive airway diseases such as chronic obstructive pulmonary disease (COPD), Bronchitis, Emphysema - Conversion to open abdominal surgery during laparoscopic cholecystectomy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Positioning the patient
The patients' vital signs, pain and analgesic drug use were recorded in the "Pain Follow-up Form" at the time they came to the clinic, at the 6th and 12th hours after the surgery, by recording from the end-of-operation file. In case the patient had pain, the time when the pain started was recorded, the experimental group was given the semi-recumbent position with analgesic drug and the patient was asked to maintain this position for 2 hours. If the patient has pain again, this position is given again. "Patient Satisfaction Evaluation Form" was filled in at the 12th hour after the surgery for the patients in the experimental group.

Locations

Country Name City State
Turkey University of Health Sciences Ankara

Sponsors (1)

Lead Sponsor Collaborator
Sibel Yilmaz Sahin

Country where clinical trial is conducted

Turkey, 

References & Publications (3)

Aydemir Ö, Aslan FE, Karabacak Ü, Akdas Ö. The Effect of Exaggerated Lithotomy Position on Shoulder Pain after Laparoscopic Cholecystectomy. Pain Manag Nurs. 2018 Dec;19(6):663-670. doi: 10.1016/j.pmn.2018.04.012. Epub 2018 Jun 19. Erratum in: Pain Manag Nurs. 2019 Feb;20(1):89. — View Citation

Pasquier EK, Andersson E. Pulmonary recruitment maneuver reduces pain after laparoscopic bariatric surgery: a randomized controlled clinical trial. Surg Obes Relat Dis. 2018 Mar;14(3):386-392. doi: 10.1016/j.soard.2017.11.017. Epub 2017 Nov 22. — View Citation

Phelps P, Cakmakkaya OS, Apfel CC, Radke OC. A simple clinical maneuver to reduce laparoscopy-induced shoulder pain: a randomized controlled trial. Obstet Gynecol. 2008 May;111(5):1155-60. doi: 10.1097/AOG.0b013e31816e34b4. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other patient's satisfaction with the given position Used Yes or No question to evaluate if patient were satisfied with the semi-recumbent position to prevent post-operative shoulder pain and Whether they think the semi-recumbent position is beneficial.
Numerical rating scale (NRS) were used to evaluate how satisfied they are with the semi-recumbent position to avoid surgery-related shoulder pain and How much discomfort they felt during their stay in the semi-recumbent position. NRS of 0 to10 were used and rated as 0 is not at all and 10 is very much
postoperative 12th hour
Primary Pain Severity Pain evaluated with numerical rating scale (NRS). A numerical rating scale requires the patient to rate their pain on a defined scale. For example, 0-10 where 0 is no pain and 10 is the worst pain imaginable arrival time at the clinic (approximately the first two hours postoperatively)
Primary Pain Region Description of pain region as
Right shoulder
Left shoulder
Both shoulder
Back
Incision
Other
arrival time at the clinic (approximately the first two hours postoperatively)
Primary Pain Severity Pain evaluated with numerical rating scale (NRS). A numerical rating scale requires the patient to rate their pain on a defined scale. For example, 0-10 where 0 is no pain and 10 is the worst pain imaginable postoperative 6th hour
Primary Pain Region Description of pain region as
Right shoulder
Left shoulder
Both shoulder
Back
Incision
Other
postoperative 6th hour
Primary Pain Severity Pain evaluated with numerical rating scale (NRS). A numerical rating scale requires the patient to rate their pain on a defined scale. For example, 0-10 where 0 is no pain and 10 is the worst pain imaginable postoperative 12th hour
Primary Pain Region Description of pain region as
Right shoulder
Left shoulder
Both shoulder
Back
Incision
Other
postoperative 12th hour
Secondary Use Analgesia Number of Analgesia used to reduce pain since arrival postoperatarrival time at the clinic (approximately the first two hours postoperatively)
Secondary Use Analgesia Number of Analgesia used to reduce pain between arrival time and 6th hour postoperative 6th hour
Secondary Use Analgesia Number of Analgesia used to reduce pain between 6th hour and 12th hour postoperative 12th hour
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