Assessing the outcomes of drain insertion in open versus laparoscopic splenectomy or splenorrhaphy in patients who are candidate for spleen surgery

Assessing the outcomes of drain insertion in open versus laparoscopic splenectomy or splenorrhaphy in patients who are candidate for spleen surgery: a clinical trial

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT201612059014N136

Enrollment

Registered

2016-12-23

Start date

2016-05-21

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

candidate for spleen surgery. Injury of spleen

Interventions

Intervention 1: Intervention group: Laparoscopic splenectomy or splenorrhaphy. Intervention 2: Control group: Open splenectomy or splenorrhaphy.

Treatment - Surgery

Intervention group: Laparoscopic splenectomy or splenorrhaphy.

Control group: Open splenectomy or splenorrhaphy.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Candidate for spleen surgery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Dehiscence. Timepoint: during the first five days after surgery. Method of measurement: through clinical examination.;Surgical wound infection. Timepoint: during the first five days after surgery. Method of measurement: through clinical examination.;Accumulation of non-purulent discharge on the surgical side. Timepoint: during the first five days after surgery. Method of measurement: through clinical examination.;Formation of sub-diaphragmatic abscess. Timepoint: on the fifth day after surgery. Method of measurement: through CT-scan.	—

Measure

Time frame

Dehiscence. Timepoint: during the first five days after surgery. Method of measurement: through clinical examination.;Surgical wound infection. Timepoint: during the first five days after surgery. Method of measurement: through clinical examination.;Accumulation of non-purulent discharge on the surgical side. Timepoint: during the first five days after surgery. Method of measurement: through clinical examination.;Formation of sub-diaphragmatic abscess. Timepoint: on the fifth day after surgery. Method of measurement: through CT-scan.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Vahid Hamzei

Besat Hospital

dr_hamzei8007@yahoo.com+98 81 3364 0030

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026