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Evaluation of Surgical Excision of Cardiophrenic Lymph Nodes in Patients With Advanced Ovarian Cancer

M

Mansoura University

Status

Unknown

Conditions

Ovarian Cancer

Treatments

Procedure: cardiophrenic lymph nodes resection

Study type

Interventional

Funder types

Other

Identifiers

NCT03235648
R/17.05.162

Details and patient eligibility

About

Evaluation of surgical excision of cardiophrenic lymph nodes in patients with advanced ovarian cancer

Full description

The role of cardiophrenic lymph node assessment and excision in advanced ovarian cancer is still debatable , correlation of radiological finding with pathological findings after reaction of radiological positive lymph nodes and its impact in diseases free survival and over all survival

Enrollment

25 estimated patients

Sex

Female

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

  • Ovarian cancer patient (FIGO stage III-IV)
  • Preoperative CT showing CPLN with short axis diameter > 5mm.
  • Anathestically fit patient (ASA score I or II).
  • Accepted pulmonary function test.
  • Patient who received neoadjuvant chemotherapy or recurrent cases may be enrolled
  • Written informed consent.
  • Achievement of optimal cytoreduction intra-abdominal( No residual disease more than 1 cm )

Exclusion Criteria:

  • Anathestically unfit patient
  • Unresectable disease
  • Patient refusal
  • No detected CPLN by preoperative radiology

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

cardiophrenic nodes excision in ovarian cancer
Experimental group
Description:
We are going to evaluate the comorbidites and impact of cardiophrenic lymph nodes excision in cases of advanced ovarian cancer with positive cardiophrenic lymph nodes
Treatment:
Procedure: cardiophrenic lymph nodes resection

Trial contacts and locations

1

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Central trial contact

Basel R. Abdelfattah, MD, MRCS

Data sourced from clinicaltrials.gov

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