Minimal Invasive Mitral Valve Replacement Versus Conventional Median Sternotomy Approach

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03195595

Enrollment

Registered

2017-06-22

Start date

2020-04-01

Completion date

2021-10-31

Last updated

2020-06-12

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

Conditions

Mitral Valve Disease

Brief summary

This is retrospective study that will be done in Cardiothoracic surgery department in Assuit university hospitals for one year duration aiming to compare minimal invasive technique to conventional median sternotomy for mitral valve surgery regarding early postoperative outcomes and pain

Detailed description

This is retrospective study that will be done in Cardiothoracic surgery department in Assuit university hospitals for one year duration and the study tools will be: Part I (Demographic data): * Age, Gender, Weight, Height ,Smoke history Part II (Preoperative data): * Medical history, Clinical assessment, Preoperative investigation Part III (Intraoperative data): * Surgical time, and Ischemic time Part IV (Postoperative data): * Early ambulation, ICU stay, length of ventilation, using of analgesic drugs, post op bleeding, deaths

Interventions

DEVICEmitral valve replacement

early postoperative outcome regarding pain in minimal invasive technique

DEVICEconventional mitral valve replacement

early postoperative outcome regarding pain in conventional median sternotomy

Study design

Observational model

CASE_CONTROL

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Symptomatic patients with mitral valve disease indicated for valve surgery

Exclusion criteria

* Double valve disease or other valve disease * Mitral or aortic valve disease associated with ischemic heart disease * Mitral or aortic valve disease associated with congenital heart disease * Patients subjected to prior heart surgery

Design outcomes

Primary

Measure	Time frame	Description
Evaluating of postoperative pain by using numerical rating scales (NRS)	one year	its a score result from gathered information from the patient

Secondary

Measure	Time frame	Description
Evaluating early postoperative outcome	one year	e.g., bleeding

Countries

Egypt

Contacts

Primary ContactElhussein abdelmottaleb, master

husseinmoh24@gmail.com00201003873076

Outcome results

None listed

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