Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT04666051 |
Other study ID # |
4/2015/SURG |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
May 2015 |
Est. completion date |
October 2020 |
Study information
Verified date |
August 2022 |
Source |
Menoufia University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Seroma is one of the most common encountered morbidities after inguinal lymph node dissection
(ILND). It can cause not only much nuisance to both patients and doctors but also its
presence can lead to many complications. This study aimed at evaluation of the role and
effect of using fibrin glue on seroma reduction in patients undergoing ILND. Thirty-two
patient have undergone ILND for various causes. The patients were randomized into two groups;
16 ILND in each. In one group, fibrin glue sealant was applied with a dose of 2ml per 100 cm2
surface area then drain placement was performed. Whereas, in the control group, only drain
placement was used. Preoperative, operative and postoperative data were recorded and
analyzed.
Description:
Seroma is one of the most frequent complications occurring after ILND as it affects nearly
one third of these cases. During the past decades, many actions have been tried in the
perioperative care to decrease the incidence of these complications, as employing well
vascularized bulky flaps to obliterate the dead space and to protect vessels, great saphenous
vein sparing, strict bed rest and fibrin sealant application. Realizing the underlying
pathology for seroma formation is the key point in its prevention. Thirty-nine patients
scheduled to perform Inguinal lymphadenectomy for various causes have been checked for
eligibility to be enrolled in this prospective, randomized study. Thirty-two patients have
met the inclusion criteria. Inguinal lymphadenectomy has been performed including scarifying
saphenous vein. Sartorius muscle transposition flap was routinely performed for protection of
femoral vessels, then an 18 French conventional non-suction tube drain was inserted in all
patients. All the previous steps were similar in both groups. At this stage, the wound was
closed for the control group, while fibrin glue was prepared to be applied to the fibrin glue
group in a dose of 2mL for 100 cm2 surface area. Postoperatively, the daily collected drain
fluid was measured till the drain was removed when the daily drainage was less than 30 ml.
Then the patients were planned to be followed up postoperatively for at least 4 weeks, to
detect the possible clinically encountered complications as seroma, wound infection, or skin
flap necrosis.
Patients' demographic data and preexisting co-morbidities were recorded. Operative and
pathological data regarding defect size, blood transfusion, primary tumor pathology, and
number and status of retrieved lymph nodes were collected. The occurrence of post-operative
seroma was the primary outcome. Other non serious adverse effect as hematoma, infection, or
skin flap necrosis were recorded and compared between the two groups.
The normality of distribution of variables was verified by Kolmogorov- Smirnov test.
Chi-square test (Fisher or Monte Carlo) was used for comparisons between groups for
categorical variables. Student t-test was used to compare two groups for normally distributed
quantitative variables. For not normally distributed quantitative variables, Mann Whitney
test was used to compare between two groups. P value was set to be significant if <0.05.