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NCT Number: NCT05874895

MAnual Lymphatic DrAinage to iMprove the outcomE of Patients After Septic Shock

Antimicrobial and supportive therapeutic interventions in patients with septic shock are usually effective - procalcitonin and interleukin-6 levels fall rapidly in most cases, and noradrenaline support can be discontinued within a few days. Unfortunately, only in a small portion of patients, do the organ functions improve at the same time, and in most of them, multi-organ failure persists. Therefore, it is likely that, in addition to infection and the response to infection, other mechanisms are also involved in the persistence of organ failure in patients after septic shock.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Ostrava

Ostrava, Moravian-Silesian Region, 708 52, Czechia

About this study

One of the possible explanations for prolonged multi-organ dysfunction after an excessive inflammatory phase is a disorder of "post-inflammatory cleaning", the so-called resolution of inflammation. The resolution of inflammation is a regulated process in which the controlling action of specialized pro-resolution mediators (lipoxins, resolvins, etc.), conversion of pro-inflammatory macrophages (M1) to pro-resolution (M2., induce the process of structural tissue restoration), autophagy plays a significant role and, of course, the flushing of accumulated interstitial fluid with waste products by lymphatic drainage. Any disturbance in pro-resolution mechanisms can lead to prolonged organ dysfunction.

The lymphatic system plays a key role in maintaining fluid homeostasis. Its ability to drain interstitial fluid can increase up to 20 times. However, even such an increase may not be sufficient in the situation of extreme interstitial fluid sequestration that accompanies septic shock. In addition, some inflammatory mediators (for example, nitric oxide, TNF-α, Interleukin-1β) cause relaxation of the vascular structures of the lymphatic system, slowing the flow of lymph. The result is the persistence of tissue swelling with tissue hypoxia due to the extension of the diffusion path for oxygen and the accumulation of waste products of inflammation.

Manual lymphatic drainage (MLD) is one of the treatments that stimulate the lymphatic system. In general, it is expected to accelerate the outflow of lymph and waste products from tissues previously affected by inflammation, accelerate the recovery of tissue function, sympatholytic effect and increase the tension of the vagus nerve. It can therefore be assumed that MLD will have a beneficial effect on the course of persistent multi-organ dysfunction in patients after therapeutically managed septic shock.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diagnosis of septic shock at admission to ICU
  • sepsis or suspicion of sepsis
  • noradrenaline support required in order to maintain mean arterial pressure ≥ 65 mmHg
  • serum lactate ≥ 2 mmol/L

Exclusion criteria

  • patients <18 years of age
  • pregnant women with septic shock, in whom the pregnancy has been preserved
  • patients with a history of heart failure with NYHA (New York Heart Association) classification ≥ III
  • patients with a history of thromboembolic events
  • patients with septic shock transferred from another department/hospital, if the length of stay at the previous workplace exceeded 72 hours
  • patients with septic shock and an inauspicious prognosis, or in the phase of withdrawal of treatment
  • patients with uncontrolled infection
  • patients with septic shock who lack informed consent
  • patients with septic shock, in whom the SOFA score decreased by more than 50% during the day following the withdrawal of noradrenaline (i.e. a subgroup of patients with a rapid improvement of the clinical course after the resolution of septic shock).

Treatment and study plan

Manual Lymphatic Drainage

Procedure

Manual lymphatic drainage massage involves gently manipulating specific areas of the body to help lymph move to an area with working lymph vessels.

usual care

Procedure

Usual care provided for patients in septic shock.

Primary outcomes

  1. Feasibility Outcome - number of patients undergoing manual lymphatic drainage procedure.

    Time frame: 12 months

    The anticipated number of patients is 2 per month.

  2. Feasibility Outcome - The percentage of patients suitable for manual lymphatic drainage procedure in whom this procedure has been performed.

    Time frame: 12 months

    It is expected that manual lymphatic drainage procedure will be performed in at least 80 per cent of patients.

  3. Safety Outcome - the percentage of cases when the manual lymphatic drainage procedure interferes with standard nursing care

    Time frame: 12 months

    interference is assumed in 0 per cent of cases

  4. Safety Outcome - incidence of the need to restart circulatory support with norepinephrine

    Time frame: 12 months

    The presumed incidence is assumed in 0 per cent of cases

  5. Safety Outcome - incidence of thromboembolic events

    Time frame: 12 months

    The presumed incidence is assumed in 0 per cent of cases

  6. Efficacy Outcome - change in SOFA (sequential organ failure assessment) score

    Time frame: 12 months

    Comparison of the SOFA score on Days 3 and 5 versus Day 0 (randomisation day)

  7. Efficacy Outcome - incidence of delirium

    Time frame: 12 months

    Incidence of delirium for the period from randomisation until discharge from ICU

  8. Efficacy Outcome - 28-day mortality

    Time frame: 12 months

    28-day mortality will be observed

Sponsors and collaborators

Lead sponsor

University Hospital Ostrava

Other

Registry information

Official study title

MAnual Lymphatic DrAinage to iMprove the outcomE of Patients After Septic Shock: A Safety and Feasibility Pilot Randomized Controlled Trial

Acronym: MADAME

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
May 25, 2023
Registry last updated
Dec 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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