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Temporary Application of Abdominal Jackson-Pratt Drain to Reduce Pain After Laparoscopic Surgery in Gynecology

Evaluation of One-hour Application of Abdominal Jackson-Pratt Drain in Order to Reduce Pain After Laparoscopic Surgery in Gynecology

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03440086
Acronym
DRAIN-1
Enrollment
94
Registered
2018-02-20
Start date
2025-06-01
Completion date
2027-06-15
Last updated
2022-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Keywords

Laparoscopic surgery, Pain, Jackson-Pratt drain

Brief summary

Recent evidence has shown that the onset and intensity of post-operative pain are significantly related to the amount of residual pneumoperitoneum at the end of the surgical procedure. In addition, the use of low pressures of carbon dioxide (CO2) for induction of the pnemoperitoneum has been associated with a reduction in post-operative pain, probably due to a lower abdominal distension and a consequent reduced compression of the pelvic, abdominal and sub-diaphragmatic pain nerve fibers. The reduction of the residual pnemoperitoneum at the end of the surgical procedure could therefore play a key role in the reduction of post-operative pain, with consequent greater comfort for the patient and reduction of the use of analgesics. In view of the available evidence, the aim of the present study is to evaluate whether the application of Jackson-Pratt drain, for one hour from the end of the surgical procedure, can significantly reduce post-operative pain and the need of analgesics in patients undergoing laparoscopic gynecological surgery.

Detailed description

Laparoscopy in gynecological surgery offers numerous advantages, such as the reduction of operative time, intra-operative blood loss, post-operative pain and the possibility of early hospital discharge and return to normal daily activities in a short time. Despite these points arewidely validated in the literature, sometimes patients undergoing laparoscopy complain of abdominal pains (although slight in intensity and temporary) in the post-operative period. In some cases, the pain is characteristically irradiated at the shoulders, due to a probable irritation/compression of the phrenic nerve that runs on the lower surface of the diaphragm. Recent evidence has shown that the onset and intensity of post-operative pain are significantly related to the amount of residual pneumoperitoneum at the end of the surgical procedure. In addition, the use of low pressures of carbon dioxide (CO2) for induction of the pnemoperitoneum has been associated with a reduction in post-operative pain, probably due to a lower abdominal distension and a consequent reduced compression of the pelvic, abdominal and sub-diaphragmatic pain nerve fibers. The reduction of the residual pnemoperitoneum at the end of the surgical procedure could therefore play a key role in the reduction of post-operative pain, with consequent greater comfort for the patient and reduction of the use of analgesics. In view of the available evidence, the aim of the present study is to evaluate whether the application of Jackson-Pratt drain, for one hour from the end of the surgical procedure, can significantly reduce post-operative pain and the need of analgesics in patients undergoing laparoscopic gynecological surgery.

Interventions

DEVICEabdominal Jackson-Pratt drain

One-hour application of abdominal Jackson-Pratt drain at the end of laparoscopic procedure.

Sponsors

Università degli Studi dell'Insubria
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Randomized controlled trial (no blinded)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Patients affected by uterine fibroids, undergoing laparoscopic surgery; * American Society of Anesthesiologists physical status classification I-II.

Exclusion criteria

* inability to express pain; * any concomitant diseases requiring upper abdominal surgery, such as cholecystectomy or adhesiolysis; * laparoscopic procedures that were converted to open surgery; * other causes of known pain; * oncological cases; * use of drugs for chronic pelvic pain or hormones in the previous 3 months (wash-out period); * application of other drainages; * intra- or post-operative complications.

Design outcomes

Primary

MeasureTime frameDescription
Pain6 hours after surgery.Pain perception, expressed as Visual Analogue Score (0-10).

Secondary

MeasureTime frameDescription
Pain12 hours after surgery.Pain perception, expressed as Visual Analogue Score (0-10).
Use of AnalgesicDuring the 48 hours after surgery.Number of requests for rescue analgesia (30 mg ketorolac tromethamine, administrated intravenously).

Countries

Italy

Contacts

Primary ContactAntonio Simone Laganà, M.D.
antoniosimone.lagana@asst-settelaghi.it3296279579

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026